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Forensic DNA Fingerprinting Kit Instruction Manual

1. 10 15 Distance mm 20 45 25 30 Student Manual as 5 Ze 40 s lt Q e Oo EO NA Post Lab Interpretation of Results 1 What are we trying to determine Restate the central question 2 Which of your DNA samples were fragmented What would your gel look like if the DNA were not fragmented 3 What caused the DNA to become fragmented 4 What determines where a restriction endonuclease will cut a DNA molecule 5 A restriction endonuclease cuts two DNA molecules at the same location What can you assume is identical about the molecules at that location 6 Do any of your suspect samples appear to have EcoRI or Psil recognition sites at the same location as the DNA from the crime scene 7 Based on the above analysis do any of the suspect samples of DNA seem to be from the same individual as the DNA from the crime scene Describe the scientific evidence that supports your conclusion TWANVIN LNAGNLS U O a gt Ww gt O a lt 46 Student Manual Extension Activity 1 Plasmid Mapping Plasmids and Restriction Enzymes This lesson will demonstrate the principles of plasmid mapping by examining restriction digestion patterns of plasmids used in the laboratory section of the kit and determining the position of restriction enzym
2. BamHI 6624 Pstl 6451 EcoRV 3309 Pstl 3613 EcoRV 5450 EcoRV 4047 Pvull 4300 Suspect 5 DNA Sample APPENDIX E 93 SOOLE Sd 9STTE lS 600CE FS CEO9T PSd ST HET Sd S870 Sd LES6I PSd v6ELI PSd SECO PSd S8091 Psd S8EFI Psd 86Cb1 PSd GESTE Sd LILII PS 1826 FS L196 FS VCS8 Sd 9895 Vd BITS Sd VTIS VS Cl6r PSd EILP VS pLev ES 098 PSd VP9E St 6C9E TiS VC8T Sd 09ST WS _cLOVy WOOF _89L6 yoo LZVLLE WOOF _v0L92 4097 _9ZZLZ 14097 lambda bacteriophage genome 48502 bp Hindi 306 Pvull 401 BamHI 276 Pstl 298 EcoRI 255 Pyull 55 APPENDIX E Scal 1366 Plasmid Parent Vector 94 Appendix F References 1 DNA Profiling Fast Becoming Accepted Tool For Identification Pamela Zurer Chemical and Engineering News Oct 10 1994 PCR means polymerase chain reaction it is a technique used to amplify small amounts of DNA in this case so that further analysis of the DNA can occur RFLP means restriction fragment length polymorphisms riff lips in biotech jargon Pieces of DNA are cut with restriction enzymes into fragments of various lengths Individuals possess variable restriction recognition sites so that two pieces of DNA from separate sources may have different fragment lengths when their DNA is cut by the same enzyme An excellent resource for the classroom teacher is Gene
3. TWANVIN S YOLONYLSNI gt z S Z 6 m v D a P gt a fe Z Instructor s Manual 16 Lesson 2 Agarose Gel Electrophoresis and Visualization of DNA Fragments Advance Preparation Objectives Prepare Hindlll lambda digest DNA marker and aliquot optional Aliquot sample DNA loading dye optional Prepare the electrophoresis chamber Dilute Fast Blast DNA strain to 1x for overnight staining or 100x concentration for quick staining Set up student and teacher workstations Time required 45 minutes What is required Hindlll lambda digest DNA marker Sample loading dye Electrophoresis chambers casting trays and combs Electrophoresis buffer 1x TAE Fast Blast DNA stain 500x Procedures 1 Prepare Hindlll lambda digest DNA marker and aliquot optional Add 20 pl of DNA sample loading dye to the stock tube containing the Hindlll lambda DNA marker Heat the marker to 65 C for 5 minutes then chill on ice this results in better separation of the marker bands Label clear micro test tubes M Aliquot 15 pl of the DNA markers containing loading dye to 8 clear micro test tubes labeled M 2 Aliquot DNA sample loading dye Label eight clean micro test tubes LD for loading dye and aliquot 50 ul of sample loading dye into each tube Distribute one tube to each team 3 Prepare the electrophoresis chamber When the agarose gel has solidified sample loading and electrophoresis can begin a When
4. When such a sequence is looked at together with its complementary sequence the group reads the same in both directions These sequences called palindromes are fairly common along the DNA molecule Restriction Enzymes Molecular Scissors Viruses called bacteriophages frequently infect bacteria These viruses inject their own DNA into bacteria and force the bacteria to multiply the DNA Bacteria have evolved restriction enzymes to cut up and destroy the invading viral DNA Bacteria prevent destruction of their own DNA by modifying certain DNA bases within the specific enzyme recognition sequence which allows them to protect their own DNA while cutting up viral DNA This could be considered a very primitive immune system Restriction enzymes search the viral DNA for specific palindromic sequences of base pairs such as GAATTC and cut the DNA at these sites The actual sequence of DNA is called a restriction site Some restriction enzymes may leave a short length of unpaired nucleotide bases called a sticky end at the DNA site where they cut whereas other restriction enzymes make a cut across both strands at the same place creating double stranded DNA fragments with blunt ends Look at the DNA sequence below 5 ee Palindrome ATTCACGCA TAAGTGCGT GTA CAT g Restriction site GTAG AATTCATTCACGCA CATCTTAA GTAAGTGCGT Fragment 1 sticky end cut Fragment 2 A restriction enzyme cut the DNA between the G and the
5. 401 Z ALIAILOW NOISNALX3 TWANVIN LNAGNLS Scal 1366 Parent Plasmid pTZ18U SOOLE BSd OSCE Sd 600ZE VS CEO9T PSd STEET Sd 8707 Sd LE86I Psd POELT Sd SETOT Sq S8091 Sa S8EbIL Sd 86Cb1 PSd OE8II Sd LILII Wad 1846 Psd L196 VS VCS8 Sa 9896 ir BITS VS VTIS Wa EL6b PSd EILH PSd YLE Wd O98E VS PP9E Sd 679 PSd VEBI PSd 09ST WS Zlery yoo B9L6E yoo LVLLE l 4007 0192 14097 9ZZLZ 14097 ge genome lambda bacteriopha 48502 bp 57 Student Manual Constructing a Plasmid Questions 1 Where is the Psti site on the pTZ18U plasmid 2 Look at plasmid S4 What segment of the lambda bacteriophage has been inserted 3 After looking at the plasmid map and also the lambda phage map can you determine how many Psi restriction sites were added to the plasmid because of the inserted lambda phage DNA fragment Note that it is possible for these extra Psil sites to have been added if the original restriction digestion was done for a short time so that not all Pst sites would have been completely cut in every piece of lambda phage DNA TWANVIN LNAGNLS m gt lt j m Z 2 O gt O lt N 4 Look at plasmid S1 What segment of lambda was added to that plasmid Were any Pst restriction sites added to the plasmid with the inserted fragment of lambda DNA 5 Now let us create a different plasmid from the paren
6. Explorer Forensic DNA Fingerprinting Kit Instruction Manual Catalog 166 0007EDU explorer bio rad com The kit is shipped at room temperature Open immediately upon arrival and store reagent bag at 20 C within 3 weeks of receipt Duplication of any part of this document is permitted for classroom use only Please visit explorer bio rad com to access our selection of language translations for Biotechnology Explorer kit curriculum For technical service call your local Bio Rad office or in the US call 1 800 4BIORAD 1 800 424 6723 Can DNA evidence solve human problems DNA fingerprinting is now used routinely to solve crimes In recent years news stories have reported how miniscule amounts of DNA have been used to identify individuals involved in incidents even many years in the past as well as exonerate innocent people from incrimi nation The power of DNA as a tool for individual identification captures students imaginations This activity provides in depth instruction about how restriction enzymes cleave DNA how electrophoresis is used to separate and visualize DNA fragments and how these techniques can be combined to obtain a DNA fingerprint Principles of restriction analysis plasmid mapping and DNA fragment size determination can also be documented with this kit Open the door to rich discussions about scientific ethical and legal implications of DNA profiling DNA fingerprinting is used in medical and forensi
7. after the restriction digest After a 24 hour incubation period are there any visible clues that the restriction enzymes may have in some way changed the DNA in any of the tubes Explain your reasoning Student Manual 30 Lesson 2 Agarose Gel Electrophoresis Laboratory Procedure Student Workstations Quantity Agarose gel electrophoresis system Agarose gel Digested DNA samples Hindlll lambda digest DNA markers DNA sample loading dye Permanent marker Pipet tips 2 20 ul Micropipet 2 20 ul Waste container Gel support film if applicable Fast Blast DNA stain 1x or 100x Large containers for destaining if applicable Foam micro test tube holder Power supply Gel staining tray Electrophoresis buffer 1x TAE Instructor s Workstation 120 ml per 2 stations 1 3 per 2 stations 1 1 1 per 2 stations 275 ml per station D a Microcentrifuge or mini centrifuge optional Rocking platform optional If performing the quick staining procedure A O UU 0 25 x TAE buffer is used for fast gel electrophoresis Refer to Appendix D for detailed information 31 Student Manual lt Z lt Z Lu m H n N Z O p 2p Lu Lesson 2 Agarose Gel Electrophoresis Laboratory Procedure 1 Obtain a prepoured agarose gel from your teacher or if your teacher instructs you to do SO prepare your own gel 2 After preparing the gel remove you
8. 74 Post Lab Thought Questions 1 What can you assume is contained within each band DNA fragments 2 If this were a fingerprinting gel then how many kinds samples of DNA can you assume were placed in each separate well APPENDIX C One 3 What would be a logical explanation as to why there is more than one band of DNA for each of the samples The DNA must have been cut into fragments by restriction enzymes 4 What probably caused the DNA to become fragmented The chemical action of the restriction enzymes cutting at specific base sequences 5 Which of the DNA samples have the same number of restriction sites for the restriction endonuclease used Write the lane numbers Lanes 2 3 and 4 CS S1 and S2 6 Which sample has the smallest DNA fragment The sample in lane 5 S3 7 Assuming a circular piece of DNA plasmid was used as starting material how many restriction sites were there in lane three Please note that the starting material was a circular piece of DNA Two sites that cut the sample into two fragments 8 From the gel drawing on page 35 which DNA samples appear to have been cut into the same number and size of fragments Lanes 2 and 4 CS and S2 9 Based on your analysis of the example gel drawing on page 35 what is your conclusion about the DNA samples in the photograph Do any of the samples seem to be from the same source If so which ones Describe the evidence that supports you
9. Sterile water 2 5 ml 1 vial m 9 Hindili lambda digest DNA size marker 0 2 ug pl 100 ul 1 vial m 10 DNA sample loading dye 1 vial Q 11 Fast Blast DNA stain 500x 100 ml 1 vial Q 12 Colored micro test tubes 2 0 ml 60 m 13 Clear micro test tubes 1 5 ml 30 m 14 Agarose powder 5 g 1 m 15 Electrophoresis buffer 50x TAE 100 ml 1 m 16 Foam micro test tube holders 16 m 17 Gel staining trays 4 m Required Accessories Number Kit V Adjustable micropipet 2 20 ul catalog 166 O506EDU 1 8 m Pipet tips 2 200 ul 5 racks of 200 catalog 223 9347EDU 1 m Horizontal electrophoresis chamber catalog 166 4000EDU 1 8 m Power supply catalog 164 5050EDU 1 4 m Adjustable micropipet 20 200 ul catalog 166 0507EDU 1 m Adjustable micropipet 100 1000 ul catalog 166 0508EDU 1 m Pipet tips 100 1000 ul 5 racks of 200 catalog 223 9350EDU 1 m Permanent markers 1 Q Microwave oven or hot plate 1 m Distilled water 1 Q 500 ml Erlenmeyer flask for microwaving agarose 1 m 500 ml flask or beaker for diluting DNA stain 1 m Ice bucket with ice 1 m Laboratory tape not Scotch 3M brand or similar tape 1 Q Optional Accessories Number Kit VV 37 C water bath catalog 166 0504EDU or Mini incubation oven catalog 166 0501EDU 1 Q Gel support film 50 sheets catalog 170 2984EDU 1 Q Microcentrifuge catalog 166 0602EDU or mini centrifuge 1 m Rocking platform catalog 166 0709EDU 1 m Refills Available Separately Fas
10. The four different nitrogenous bases are adenine thymine guanine and cytosine A T G and C Remember the base pairing rule is A T and G C Refer to the figures below to review the structure of a DNA molecule Fig 1 The Structure of DNA DNA MOLECULE 1 DNA MOLECULE 2 DNA MOLECULE 3 If asegment of DNA is diagrammed without the sugars and phosphates the base pair sequence might appear as Read to the right gt ACTCCGTAGAATTC gt lt TGAGGCATCTT A AG lt Read to the left Look at the linear sequence of bases As Ts etc on each of the strands 1 Describe any pattern you might see in the upper sequence of bases 2 Compare the bases in the upper portion of the molecule to those in the lower portion Describe any relationship you can see 3 Now look at the upper sequence of bases and compare it to the lower Do you notice any grouping of bases that when read toward the right on the upper strand and read to the left on the bottom strand are exactly the same APPENDIX B 63 g XIGNAddV You may have discovered that the sequence of base pairs is seemingly random and that the two strands are complementary to each other As are paired with Ts and Cs are paired with Gs You may have also noticed that a portion of the top strand GAATTC read toward the right has a counterpart in the lower strand CTTAAG read toward the left Example sequences are GAATTC AAGCTT CTGCAG CTTAAG TTCGAA GACGTC
11. a radioactive complementary DNA probe can be made that will recognize and bind that sequence Radioactive probes allow molecular biologists to locate identify and compare the DNA of different individuals This probe can be described as a radioactive tag that will bind to a single stranded DNA fragment and produce a band in a gel or a band on a piece of blotting membrane that is a replica of the gel also known as a Southern blot Because of its specificity the radioactive probe can be used to demonstrate genotypic similarities between individuals In DNA fingerprinting the relative positions of radiolabeled bands in a gel are determined by the size of the DNA fragments in each band The size of the fragments reflect variations in individuals DNA The evidence needed for DNA fingerprinting can be obtained from any biological material that contains DNA body tissues body fluids blood and semen hair follicles etc DNA analysis can even be done from dried material such as blood stains or mummified tissue If a sample of DNA is too small it may be amplified using PCR techniques The DNA is then treated with restriction enzymes that cut the DNA into fragments of various length Instructor s Manual lt Z lt o o O jt O 2 o 2 Z m zZ O oc O x O lt m u gt O A Q D O Cc zZ g TWANVIN S HOLONULSNI Restriction Digestion of DNA Because they cut DNA restriction enzymes are the
12. chemical scissors of the molecular biologist When a particular restriction enzyme recognizes a particular recognition sequence four or six base pair bp on a segment of DNA it cuts the DNA molecule at that point The recognition sequences for two commonly used enzymes EcoRI and Psi are shown below The place on the DNA backbones where the DNA is actually cut is shown with a lt symbol GIAAATTC For the enzyme EcoRI CTTA AIG A C TGC AJG For the enzyme Ps G CGTC Like all enzymes restriction enzymes function best under specific buffer and temperature conditions The proper restriction enzyme buffer has been included with the DNA sample in this kit so that when the rehydrated DNA and enzymes are mixed the ideal conditions are created for the enzymes to function optimally The final reaction buffer consists of 50 mM Tris 100 mM NaCl 10 mM MgCl 1 mM DDT pH 8 0 which is the ideal condition for EcoRI and Psi enzymes to function Making DNA Visible DNA is colorless so DNA fragments in the gel cannot be seen during electrophoresis A sample loading buffer containing two bluish dyes is added to the DNA samples The loading dye does not stain the DNA itself but makes it easier to load the samples and monitor the progress of the DNA electrophoresis The dye fronts migrate toward the positive end of the gel just like the DNA fragments Bromophenol blue the faster dye comigrates with DNA fragments of approximately 500 bp
13. oA Za TWANVIN S YOLONYLSNI gt z S Z 6 m v D 5 gt a fe Z Making DNA Visible Fast Blast DNA stain is a convenient safe and nontoxic alternative to ethidium bromide for the detection of DNA in agarose gels following electrophoresis Fast Blast contains a cationic compound that is in the thiazin family of dyes The positively charged dye molecules are attracted to and bind to the negatively charged phosphate groups on DNA molecules The proprietary dye formula stains DNA deep blue in agarose gels and provides vivid consistent results and detects as little as 50 nanograms of DNA Fast Blast DNA stain is provided as a 500x concentrate that must be diluted prior to use The stain can be used as a quick stain when diluted to a 100x concentration to allow the visualization of DNA within 12 15 minutes or used as an overnight stain when diluted to 1x concentration When the agarose gel is immersed in Fast Blast DNA stain the dye molecules attach to the DNA molecules trapped in the agarose gel When the DNA bands are visible your students can compare the DNA restriction patterns of the different samples of DNA Detailed instructions on using Fast Blast are included in the student manual WARNING Although Fast Blast DNA stain is nontoxic and noncarcinogenic latex or vinyl gloves should be worn while handling the stain or stained gels to keep hands from becoming stained blue Lab coats or other protective clothing s
14. 11 12 13 Determining effectiveness of bone marrow transplants DNA fingerprinting can help doctors to monitor bone marrow transplants Leukemia is a cancer of the bone marrow and the diseased marrow must be removed The bone marrow makes new blood cells so the leukemia sufferer will die without a transplant of healthy marrow Doctors can quickly tell whether the transplant has succeeded by DNA typing of the patient and the donor If the transplant has worked a fingerprint from the patient s blood shows the donor s bands But if the cancerous bone marrow has not been properly destroyed then the cancerous cells multiply rapidly and the patient s own bands predominate Our Ultimate Identity Card in Sickness and in Health in Inside Science New Scientist Nov 16 1991 Proving relatedness of immigrants DNA fingerprinting has been used as proof of paternity for immigration purposes In 1986 Britain s Home Office received 12 000 immigration applications from the wives and children of Bangladeshi and Pakistani men residing in the United Kingdom The burden of proof is on the applicant but establishing the family identity can be difficult because of sketchy documentary evidence Blood tests can also be inconclusive but DNA fingerprinting results are accepted as proof of paternity by the Home Office DNA fingerprints source unknown Based on A J Jeffreys et al Positive Identification of an Immigration Test Case Using Hum
15. A in a GAATTC palindrome 4 How many bases are still paired to the left of the cut 5 How many bases are still paired to the right of the cut 6 Counting the number of paired bases is the right fragment the same size as the left fragment 7 How could you describe the size of each fragment in terms of the number of base pairs in the fragment 64 An important feature of restriction enzymes is that each enzyme only recognizes a specific palindrome and cuts the DNA only at that specific sequence of bases A palindromic sequence can be repeated a number of times on a strand of DNA and the specific restriction enzyme will cut all those palindromes no matter what species the DNA comes from 8 If the GAATTC palindrome is repeated four times on the same piece of linear DNA and the restriction enzyme that recognizes that base sequence is present and digests the DNA how many DNA fragments will be produced 9 If the GAATTC palindrome repeats are randomly found along the DNA strand then what can you say about the sizes of the fragments that will be produced when the DNA is digested with a restriction enzyme that recognizes that sequence The table below shows palindromic sequences that are recognized by the enzymes that are used to digest the DNA you will be analyzing in this activity Palindromic sequence Name of restriction enzyme that recognizes the palindrome GAATTC CTTAAG AAGCTT TTCGAA CTGCAG GACGTC
16. EcoRI Hindili Pst 65 APPENDIX B ga XIGNAddV Below is the summary of what we have learned so far e Asequence on one strand of DNA and its complementary sequence on the other strand can form a palindrome i e GAATTC CTTAAG e Palindromes can be detected by restriction enzymes e Restriction enzymes cut the palindromes at restriction sites e Restriction enzymes recognize specific palindromes e Cutting DNA at restriction sites will produce DNA fragments e Fragment size can be described by the number of base pairs a fragment contains Applying What You Have Learned A linear DNA molecule is represented below The DNA is represented by one line although in actuality DNA has two strands 1 Ifthe DNA molecule has two restriction sites for restriction enzyme A how many fragments would be produced if the DNA is cut by that enzyme A A 2 Number each fragment 3 Which fragment is the largest 4 Which fragment is the smallest 66 5 Draw a DNA molecule that has five randomly spaced restriction sites for a specific palindrome How many fragments would be produced if each site were cut by that specific restriction enzyme 6 Label each fragment 7 Rank them in order of size from largest to smallest A l 4 In this diagram A and B are different palindrome sequences on a DNA strand Only the restriction enzyme that recognizes site B is present 8 Explain why only two fragments would be produced AP
17. as was seen a A 2 817 2 4 roa EcoRI lt Pst Pst Pst 820 Pst 820 43 EcoRI EcoRI 3 687 3 687 12 When the gels were run for this experiment there were only three bands for plasmid S3 Which band is missing from your gel Why The 43 bp band is so small that it does not bind enough Fastblast stain to be visible or it may have run off the gel 83 XIGNAddV Extension Activity 2 Constructing a Plasmid Questions 1 Where is the Psi site on the pTZ18U plasmid Position 298 Look at plasmid S4 What segment of the lambda bacteriophage has been inserted Lambda fragment 5 218 9 617 was added After looking at the plasmid map and also the lambda phage map can you determine how many Pst restriction sites were added to the plasmid because of the inserted lambda phage DNA fragment Note that it is possible for these extra Pst sites to have been added if the original restriction digestion was done for a short time so that not all Pstl sites would have been completely cut in every piece of lambda phage DNA Two restriction sites for Psi were added site 766 and site 3 604 Look at plasmid S1 What segment of lambda was added to that plasmid Were any Pstl restriction sites added to the plasmid with the inserted fragment of lambda DNA Lambda fragment 20 285 22 425 was added to plasmid S1 No additional Psa sites were added Now let us create a different plasmid from the parent plasmid You will use EcoRI for the constructio
18. explanation 59 Student Manual V XIGNAddV Appendix A Alternative DNA Fingerprinting Scenarios DNA typing DNA profiling and DNA fingerprinting are all names for the same process a process that uses DNA to show relatedness or identity of individual humans plants or animals DNA typing has become the subject of much debate and interest because of its uses for forensics analysis in prominent criminal cases such as the O J Simpson case The applications of DNA typing however are much broader than forensic science alone and are having a profound impact on our society DNA typing is used in forensics anthropology and conservation biology not only to determine the identity of individuals but also to determine relatedness This process has been used to free innocent suspects reunite children with their relatives identify stolen animals and prove that whale meat has been substituted for fish in sushi It is used in times of war to help identify the remains of soldiers killed in combat It is also being used to find genetic linkages to inherited diseases In addition scientists are learning a great deal about our evolutionary history from DNA analysis Each of the following paragraphs describes a scenario in which DNA has been used to show how individuals are related to each other or to show that a person is or is not the perpetrator of a crime These scenarios provide a context for using DNA typing for use in teaching molecular b
19. gt Z Cc gt I 4 DNA fragment size can be expressed as the number of base pairs in the fragment Indicate the size of the fragments mention any discrepancy you may detect a The smaller fragment is base pairs bp b What is the length of the longer fragment 5 Consider the two samples of DNA shown below single strands are shown for simplicity Sample 1 CAGTGATCTCGAATTCGCTAGTAACGTT Sample 2 TCATGAATTCCTGGAATCAGCAAATGCA If both samples are treated with the restriction enzyme EcoRI recognition sequence GAATTC then indicate the number of fragments and the size of each fragment from each sample of DNA Sample 1 Sample 2 of fragments of fragments gt smallest List fragment size in order largest Sample 1 Sample 2 Student Manual 26 Lesson 1 Restriction Digestion of DNA Samples Upon careful observation it is apparent that the only difference between the DNA of different individuals is the linear sequence of their base pairs In the lab your team will be given 6 DNA samples Recall that your task is to determine if any of them came from the same individual or if they came from different individuals Thus far you have learned the following e The similarities and differences between the DNA from different individuals e How restriction endonucleases cut hydrolyze DNA molecules e How adding the same restriction endonuclease to two samples of DNA might provide some clues abou
20. known standards The sizes of the fragments from the single digests and the double digest are determined then logic is used to assess the relative location of restriction sites Instructor s Manual Instructor s Advance Preparation Guide Implementation Timeline There are four activities and two optional extension activities in this fingerprinting curriculum All activities are designed to be carried out in consecutive 50 minute periods Activities include e A series of prelab considerations for students e An active student investigation e Questions for analysis and interpretation of lab results Student Schedule Pre Lab Activity Activity Lesson 1 Activity Lesson 2 Activity Post Lab Activity Activity Introduction to DNA Fingerprinting Lecture and discussion Prelab considerations 1 and 2 Restriction Digest of DNA Samples Pour gels perform the restriction digests Complete preliminary analysis and review questions Electrophoresis of DNA Samples Load and run gels stain gels Do analysis and review questions Analysis and Interpretation of Results Do analysis questions Generate standard curve Discuss results and weigh evidence Extension Activities Activity 1 Activity 2 Plasmid Mapping Work through questions Constructing a Plasmid Work through questions JIZ gO Zq T Oth co Oa OO gt 22 rea Ks MO Zq Instructor s Manual Instructor s Advance Preparation T
21. off the stain into a waste beaker d Record results e Trim away any unloaded lanes y f Air dry the gel on gel support film and tape the dried gel into your laboratory notebook Student Manual 22 Student Manual Pre Lab Introduction to DNA Fingerprinting You are about to perform a procedure known as DNA fingerprinting The data obtained may allow you to determine if the samples of DNA that you will be provided with are from the same individual or from different individuals For this experiment it is necessary to review the structure of DNA molecules DNA consists of a series of nitrogenous base molecules held together by weak hydrogen bonds These base pairs are in turn bonded to a sugar phosphate backbone The four nitrogenous bases are adenine thymine guanine and cytosine A T G and C Remember the base pairing rule is A T and G C Refer to the figure below of a DNA molecule The Structure of DNA DNA MOLECULE 1 DNA MOLECULE 2 DNA MOLECULE 3 The schematics above represent a very small section of DNA from three different individuals In this representation of DNA the symbol system is as follows Backbone S Five carbon sugar molecule known as deoxyribose P Phosphate group DNA Nucleotide Bases A adenine C cytosine G guanine T thymine Analysis of the three DNA samples above see next page might help us detect similarities and differen
22. placing the gel tray into the electrophoresis chamber make sure that the sample wells are at the black cathode end DNA samples will migrate toward the red anode end during electrophoresis Make sure the tray is fully seated in the chamber b Prepare the required volume of 1x TAE buffer if you have not prepared it already c Submerge the gel under about 2 mm of 1x TAE buffer d Prepare samples for gel loading See laboratory protocol in the student section Note Power requirements vary depending on gel thickness length and concentration and on type of electrophoresis buffer used For this exercise we recommend using a constant voltage of 100 V for 30 min See Appendix D for a faster electrophoresis protocol which allows the gel to be run in 20 min 4 Prepare Fast Blast DNA stain a To prepare 100x stain for quick staining dilute 100 ml of 500x Fast Blast with 400 ml of distilled or deionized water in an appropriately sized flask or bottle and mix Cover the flask and store at room temperature until ready to use b To prepare 1x stain for overnight staining dilute 1 ml of 500x Fast Blast with 499 ml of distilled or deionized water in an appropriately sized flask or bottle and mix Cover the flask and store at room temperature until ready to use 0 25 x TAE buffer is used for fast gel electrophoresis Refer to Appendix D for detailed information Instructor s Manual 17 JZ Z2 Zq F o fs Pw CoO gt 22 cea E gt
23. sketched or retained as a permanently dried gel for analysis Detained instruction on staining your gel are found on the following pages The drawing below represents an example of a stained DNA gel after electrophoresis For fingerprinting analysis the following information is important to remember e Each lane has a different sample of DNA e Each DNA sample was treated with the same restriction endonucleases With reference to the numbered lanes analyze the bands in the gel drawing below then answer the questions on page 40 Note that this picture is an example and it may not correspond to the pattern of bands that you will see in the lab cs Si Sy 8 Student Manual 35 l lt 2 Z lt Z Lu a H 2 N Z O V e9 W j m W e O Z N i Cc s m Z gt Z c gt Staining DNA with Fast Blast DNA Stain Laboratory Procedure There are two protocols for using Fast Blast DNA stain in the classroom Use option 1 for quick staining of gels to visualize DNA bands in 12 15 minutes and option 2 for overnight staining Depending on the amount of time available your teacher will decide which protocol to use Two student teams will stain the gels per staining tray you may want to notch gel corners for identification Mark staining trays with initials and class period before beginning this activity WARNING Although Fast Blast DNA stain is nontoxic and noncarci
24. temperature after 2 3 days The result will be a flat transparent and durable record for the experiment l lt 2 Z lt Z Lu a H 2 N Z O V e9 W j Gel support film Student Manual 37 m N e O Z N Cc s m Z gt Z c gt 2 Protocol 2 Overnight Staining of Agarose Gels in 1x Fast Blast DNA Stain For overnight staining Fast Blast DNA stain 500x should be diluted to a 1x concentration We recommend using 120 ml of 1x Fast Blast to stain two 7 x 7 cm or 7 x 10 cm agarose gels in individual staining trays provided in Bio Rad s education kits If alternative staining trays are used add a sufficient volume of staining solution to completely submerge the gels Following DNA electrophoresis agarose gels must be removed from their gel trays before being placed in the staining solution This is easily accomplished by holding the base of the gel tray in one hand and gently pushing out the gel with the thumb of the other hand Because the gel is fragile special attention must be given when handling it 1 Label the staining tray with your initials and class period You will stain 2 gels per tray 2 Stain gels overnight Pour 1x stain into a gel staining tray Remove the gel from the gel tray and carefully slide it into the staining tray containing the stain If necessary add more 1x staining solution to completely submerge the gels Place the stainin
25. want to draw a light pencil mark from the x axis up to the standard curve and over to the y axis showing what you ve done Where the graph line meets the y axis this is the approximate size of your unknown DNA fragment Do this for all crime scene and suspect fragments 5 Compare the fragment sizes of the suspects and the crime scene Is there a suspect that matches the crime scene How sure are you that this is a match 42 Student Manual ALIALLOV V1 LSOd TWANVIN LNAGNLS Electrophoresis data Measure the distance in millimeters that each fragment traveled from the well and record it in the table Estimate its size in base pairs by comparing its position to the Hindlll lambda DNA markers Remember some lanes will have fewer than 6 fragments Lambda Hindlll size marker Actual i Approx Distance Approx i Approx i Approx i Approx i Approx size bp size bp mm size bp size bp size bp size bp size bp Student Manual 43 TWANVIN LNAGNLS U O T gt Ww gt O a lt Size base pairs 100 000 10 000 1 000 100 Student Manual Semilog Graph Paper 10 15 20 Distance mm 44 25 30 Size base pairs 25 000 20 000 15 000 10 000 5 000 Graph Paper
26. 1 Describe the samples of DNA physical properties 2 Is there any observable difference between the samples of DNA 3 Describe the appearance of the restriction endonuclease mix 4 Combine and react Using a new pipet tip for each sample pipet 10 ul of the enzyme mix ENZ to each reaction tube as shown below Pipet up and down carefully to mix well m N e O Z n Cc g m Z gt Z Cc gt Note Change tips whenever you switch reagents or if the tip touches any of the liquid in one of the tubes accidentally When in doubt change the tip DNA goes in the tube before the enzyme Always add the enzyme last g g g g cS Si S2 S3 S4 S5 Now your DNA samples should contain Total DNA Samples EcoRI Pst Reaction 10 pl each Enzyme Mix Volume Crime Scene CS 10 ul 20 ul Suspect 1 S1 10 ul 20 ul Suspect 2 S2 10 ul 20 ul Suspect 3 S3 10 ul 20 ul Suspect 4 S4 10 ul 20 ul Suspect 5 S5 10 ul 20 ul Student Manual 28 5 Mix the tube contents Tightly cap on each tube Mix the components by gently flicking the tubes with your finger If there is a centrifuge available pulse the tubes for two seconds to force the liquid into the bottom of the tube to mix and combine reactants Be sure the tubes are in a BALANCED arrangement in the rotor If your lab is not equipped with a centrifuge briskly shake the tube once is sufficient like a thermometer Tapping the t
27. 1 from questions 8 and 9 above The double digests will show the same bands with either orientation but the Psi single digest will be different In the first orientation it will give two fragments of 4016 bp and 3722 bp In the second orientation it will give two bands at 6492 bp and 1242 bp 85 APPENDIX C XIGNAddV Prelab Activity 1 A Review of Restriction Enzymes from Appendix B 1 Describe any pattern you might see in the upper sequence of bases There is no specific type of pattern associated with the upper sequence of bases 2 Compare the bases in the upper DNA strand to those in the lower strand Describe any relationship you can see A always pairs with T G always pairs with C 3 Now look at the upper sequence of bases and compare it to the lower Do you notice any grouping of bases that when read toward the right on the upper strand and read to the left on the bottom strand are exactly the same CTTAAG 4 How many base pairs are there to the left of the cut 4 5 How many base pairs are there to the right of the cut 10 6 Counting the number of base pairs is the right fragment the same size as the left fragment No it is larger 7 How could you describe the size of each fragment in terms of the number of base pairs in the fragment Fragment 1 is a 4 base pair fragment Fragment 2 is a 10 base pair fragment 8 If the GAATTC palindrome is repeated four times on the same piece of linear DNA an
28. 24 mm mark on the x axis read up to the standard line when you intersect your standard curve mark the spot with a shaded circle B Follow the intersect point over to the y axis and determine where the graph line meets the y axis this is the approximate size of the fragment C Therefore suspect 5 band 2 is approximately 2 000 bp Repeat this procedure for the crime scene and all suspects fragments As you determine the approximate fragment sizes fill in the data in the data table 77 XIGNAddV Size base pairs 25 000 20 000 15 000 10 000 5 000 Fingerprinting Standard Curve Linear 10 15 20 25 Distance mm 78 30 Post Lab Activity Interpretation of Results 1 What are we trying to determine Restate the central question We are trying to determine if samples of DNA that we were provided with are from the same individual or from different individuals APPENDIX C Which of your DNA samples were fragmented What would your gel look like if the DNA were not fragmented The number of fragmented samples will vary They will have one band on the gel if the DNA was not cut What caused the DNA to become fragmented The addition of restriction enzymes What determines where a restriction endonuclease will cut a DNA molecule A sp
29. 5 Lane 6 Lane 7 Hindlll DNA size marker clear tube 10 ul CS green tube 20 ul S1 blue tube 20 ul S2 orange tube 20 ul S3 violet tube 20 pl S4 red tube 20 ul S5 yellow tube 20 ul 7 Secure the lid on the gel box The lid will attach to the base in only one orientation red to red and black to black Connect electrical leads to the power supply 8 Turn on the power supply Set it for 100 V and electrophorese the samples for at least 30 min The gel can be run for up to 40 min to improve resolution if the time is available The Fast Gel Protocol in Appendix D allows the gel to be run in 20 min at 200 V While you are waiting for the gel to run you may begin the review questions on the following page 9 When the electrophoresis is complete turn off the power supply and remove the lid from the gel box Carefully remove the gel tray and the gel from the electrophoresis a lt Z lt Lu m H n N Z O 7 Ww chamber Be careful the gel is very slippery Proceed to pg 35 for detailed instructions on staining your gel Student Manual 33 Lesson 2 Agarose Gel Electrophoresis Review Questions 1 The electrophoresis apparatus creates an electrical field with positive and negative poles at the ends of the gel DNA molecules are negatively charged To which electrode pole of the electrophoresis field would you expect DNA to migrate or Explain 2 What col
30. 8 however only 6 will be large enough to appear on the gel 6 On the gel diagram show how you believe these fragments will sort out during electrophoresis The two fragments with no length indicated will be too small to be visualized on the gel Well Negative 23 130 9 416 6 557 4 361 2 322 Positive t 7 Label each fragment with its correct number of base pairs See gel above 89 a XIGNAddV Appendix D Fast Gel Protocol The DNA Fingerprinting gels can be run in under 20 minutes by using a reduced concentration of running buffer 0 25x TAE the same concentration of buffer in the gel itself 1x TAE and higher voltage 200 volts Resolution is excellent and the gel can be run 33 faster The provided 50x TAE buffer is mixed with distilled water to yield the necessary concentrations for making agarose gels and electrophoresis running buffer Use 1x TAE to make agarose gels Half a liter of 1x TAE is sufficient to make eight 7 x 10 cm agarose gels To make 500 ml of 1x TAE from a 50x TAE concentrate add 10 ml of concentrated TAE to 490 ml of distilled water For added convenience precast 1 agarose gels made with 1x TAE are available from Bio Rad catalog 161 3057EDU Use 0 25x TAE to make electrophoresis running buffer A 2 5 liter volume of 0 25x TAE buffer is required to run eight 7 x 10 agarose gels To make 2 5 L of 0 25x TAE from a 1x TAE solution add 625 ml of 1x TAE to 1 875 ml of distilled water N
31. Draw the Psd fragment that is cut with EcoRI in plasmid S5 to demonstrate how the fragment was cut with EcoRI 2 860 43 h 2 817 EcoRI 81 XIGNAddV 7 Restriction mapping is an exercise in critical thinking and logic Plasmid S5 is difficult to completely map because of the numerous Psi restriction sites With the data it would be very difficult to place all the restriction sites in order It is easier to map plasmid S3 How many times did EcoRI cut plasmid S3 What are the fragment sizes EcoRi cut plasmid S3 twice The fragments are 863 and 6505 bp in size 8 The data from the EcoRI digest of plasmid S3 indicate that the fragments are not equal Draw a possible map and label the EcoRI sites and the sizes of the fragments EcoRI 863 6 504 EcoRI 9 Now draw an approximate map of the Pst sites on plasmid S3 and label the Pst sites and the sizes of the fragments 2 860 Pst Pstl 4 507 10 Draw a circular map of plasmid S3 digested with both Psil and EcoRI Mark sizes of each fragment and name the restriction sites on your figure 2 817 EcoRI 43 Pst Pst 820 EcoRI 3 687 11 Is there another possible order of restriction sites on plasmid S3 digested with both Pst and EcoRI How might you resolve these possibilities O Using the data from the double digest there are two possibilities see diagram x lt However the single digest with Psi would have fragments of 3687 and 3637 bp Q not 4507 and 2860 bp
32. I Mark sizes of each fragment and name the restriction sites on your figure 11 Is there another possible order of restriction sites on plasmid S3 digested with both Pst and EcoRI How might you resolve these possibilities 12 When the gels were run for this experiment there were only three bands for plasmid S3 Which band is missing from your gel Why Student Manual 54 Extension Activity 2 Constructing a Plasmid Some plasmids replicate when the bacterial genomic DNA replicates but others replicate independently producing hundreds of copies of the plasmid within one cell A self replicating plasmid contains its own origin of replication Ori Many plasmids also contain genes that give antibiotic resistance to bacteria Plasmids are made of DNA just like the bacterial genome Since DNA is universal in all living things plasmids with inserted foreign DNA may be put into a bacteria transforming them causing the bacteria to transcribe and translate that message into a protein product The biotech industry is in part based on this principle Bacteria can be given human genes via a plasmid and once transformed can produce a human protein product This exercise is based on plasmids used in the forensic DNA fingerprinting lab Five plasmids were constructed from a parent plasmid and then were cut digested to make fragments of different sizes for a gel analysis How were the plasmids constructed Could one have made the plasmids dif
33. IN S YOLONULSNI gt z gt Z 6 m v D D gt gt o Z Lesson 2 Electrophoresis of DNA Samples Materials Needed for Each Workstation Quantity Agarose gel electrophoresis system 1 Agarose gel 1 Digested DNA samples 6 Hindlll lambda digest DNA marker 1 DNA sample loading dye 1 Permanent marker 1 Pipet tips 2 20 ul 13 Adjustable micropipet 2 20 ul Waste container Gel support film if applicable Fast Blast DNA stain 1x or 100x Large containers for destaining if applicable Foam micro test tube holder Power supply Gel staining tray Electrophoresis buffer 1x TAE Instructor s Workstation 120 ml per 2 stations 1 3 per 2 stations 1 1 1 per 2 stations 275 ml per station Microcentrifuge or mini centrifuge optional Rocking platform optional Post Lab Activity Analysis of Results Materials Needed for Each Workstation Quantity Millimeter ruler Semilog graph paper Gel support film if applicable Instructor s Workstation 1 1 1 None required COOOOCOCOCOCOCOOCODOR DDOD 00 OR Depending on whether the quick or overnight staining will be followed Instructor s Manual 12 Instructor s Advance Preparation for Labs This section describes the preparation that needs to be performed by the instructor before each laboratory An estimation of preparation time is included in each section Lesson 1 Restriction Digestion of DNA Sampl
34. PENDIX B 67 g XIGNAddV Prelab Activity 2 A Review of Electrophoresis Agarose gel electrophoresis is a procedure used to separate DNA fragments based on their sizes DNA is an acid and has many negative electrical charges Scientists have used this fact to design a method that can be used to separate pieces of DNA A solution containing a mixture of DNA fragments of variable sizes is placed into a small well formed in an agarose gel that has a texture similar to gelatin An electric current causes the negatively charged DNA molecules to move towards the positive electrode Imagine the gel as a strainer with tiny pores that allow small particles to move through it very quickly The larger the size of the particles however the slower they are strained through the gel After a period of exposure to the electrical current the DNA fragments will sort themselves out by size Fragments that are the same size will tend to move together through the gel and form bands A piece of DNA is cut into four fragments as shown in the diagram fiagatis A solution containing the four Well fragments is placed in a well in an agarose gel Using the information given above draw to the right how you think the fragments might be separated Label each fragment with its corresponding letter lt _ A B c D Positive Agarose gel m Have your teacher check your diagram before you proceed 1 Where would the larger fragments those with t
35. Predict what fragments you would generate if you were to digest your plasmid with EcoRI alone Two fragments in each case since there are two EcoRI sites POSSIBILITY 1 Lambda 21 226 26 104 4878 2860 Pst alone POSSIBILITY 2 Lambda 26 104 31 747 5643 2860 POSSIBILITY 3 Lambda 39 168 44 972 5804 2860 Two fragments for possibility 1 amp 2 and one fragment with possibility 3 POSSIBILITY 1 Lambda 21 226 26 104 4016 3722 POSSIBILITY 2 Lambda 26 104 31 747 4858 3645 EcoRI and Psil together a double digest Four fragments for possibility 1 and 2 and three fragments with possibility 3 POSSIBILITY 3 Lambda 39 168 44 972 8664 POSSIBILITY 1 POSSIBILITY 2 POSSIBILITY 3 Lambda Lambda Lambda 21 226 26 104 26 104 31 747 39 168 44 972 3679 4815 5804 2817 2817 2817 1199 828 43 43 43 Draw an agarose gel for each of these digests and label the fragment sizes POSSIBILITY 1 POSSIBILITY 2 POSSIBILITY 3 EcoRI Pst Both EcoRI Psi Both EcoRI Psa Both 8664 5804 5804 5643 4878 4858 4815 3722 3679 2860 2817 2860 2817 2860 2817 1199 828 10 The band at 43 bp is too small to be seen The lambda phage fragment can be inserted into the host plasmid in either orientation forwards or backwards How could you use plasmid mapping to determine in which orientation your fragment was inserted Use a diagram in your explanation Using possibility
36. Using a ruler measure the distance in mm that each of your DNA fragments or bands traveled from the well Measure the distance from the bottom of the well to the center of each DNA band and record your numbers in the table on the next page The data in the table will be used to construct a standard curve and to estimate the sizes of the crime scene and suspect restriction fragments 2 To make an accurate estimate of the fragment sizes for either the crime scene or suspect DNA samples a standard curve is created using the distance x axis and fragment size y axis data from the known Hindlll lambda digest DNA marker Using both linear and semilog graph paper plot distance versus size for bands 2 6 On each graph draw a line of best fit through the points Extend the line all the way to the right hand edge of the graph Which graph provides the straightest line that you could use to estimate the crime scene or the suspects fragment sizes Why do you think one graph is straighter than the other 3 Decide which graph linear or semilog should be used to estimate the DNA fragment sizes of the crime scene and suspects Justify your selection 4 To estimate the size of an unknown crime scene or suspect fragment find the distance that fragment traveled Locate that distance on the x axis of your standard graph From that position on the x axis read up to the standard line and then follow the graph line to over to the y axis You might
37. a group of enzymes in bacteria which when added to any DNA will result in the breakage hydrolysis of the sugar phosphate bond between certain specific nucleotide bases recognition sites This causes the double strand of DNA to break along the recognition site and the DNA molecule becomes fractured into two pieces These molecular scissors or cutting enzymes are restriction endonucleases Two common restriction enzymes endonucleases are EcoRI and Pstl which will be provided to you in this lab procedure To better understand how EcoRI and Pstl may help you in performing your DNA fingerprinting experiment first you must understand and visualize the nature of the cutting effect of a restriction endonuclease on DNA ATGIAATTCTCAATTACCT TACTTAAIGAGTTAATGGA The line through the base pairs represents the sites where bonds will break if the restriction endonuclease EcoRI recognizes the site GAATTC The following analysis questions refer to how a piece of DNA would be affected if a restriction endonuclease were to cut the DNA molecule in the manner shown above 1 How many pieces of DNA would result from this cut 2 Write the base sequence of the DNA fragments on both the left and right side of the cut Left Right 3 What differences are there in the two pieces Student Manual 25 lt Z lt H Z Lu a H 2 Z O 177 2 Ww m wn wo O on Cc s m Z
38. an DNA Fingerprints Nature vol 317 818 819 1985 Confirming relatedness among animals Scientists who extracted DNA from the hair of chimpanzees throughout Africa now have evidence that there might be a third species of chimpanzee At the same time they have learned things about chimp behavior and kinship patterns that would have once taken years to theorize They discovered a group of chimps living in western Africa to be genetically distinct from the chimps living in other parts of Africa suggesting that the group may be an endangered species The have discovered that male chimps living in a given area are often as closely related as half brothers and many so called sub species may all be part of a single species The male chimps relatedness may explain why unlike other primates the males are quite friendly to each other DNA testing of plant material puts murderer at the scene Two small seed pods caught in the bed of his pick up truck put an accused murderer at the murder scene Genetic testing showed that DNA in the seed pod exactly matched the DNA of a plant found at the scene of the murder The accused had admitted he had given the victim a ride but he denied ever having been near the crime scene 62 Appendix B Prelab Activity 1 A Review of Restriction Enzymes DNA consists of a series of nitrogenous base molecules held together by weak hydrogen bonds These base pairs are in turn bonded to a sugar phosphate backbone
39. andling Be sure to use electrophoresis buffer not water to prepare agarose gels See Appendix D for alternative Fast Gel Protocol a Electrophoresis buffer preparation TAE Tris acetate EDTA electrophoresis buffer is provided as a 50x concentrated solution In addition to the 1x TAE buffer needed to make the agarose gels approximately 275 ml is also required for each electrophoresis chamber Three liters of 1x TAE buffer will be sufficient to run 8 electrophoresis chambers and prepare 8 agarose gels To make 3 L of 1x TAE from 50x TAE concentrate add 60 ml of 50x concentrate to 2 94 L of distilled water b Agarose preparation These procedures may be carried out 1 to 2 days ahead of time by the teacher or done during class by the individual student teams i To make a 1 agarose solution use 1 gram of agarose for each 100 ml of 1x TAE electrophoresis buffer Be sure to use electrophoresis buffer not water If electrophoresis chambers are limiting you can use a 7 x 10 cm tray and two 8 well combs to pour a gel that can be used to run two sets of student digests Use this table as a guide for gel volume requirements when casting single or multiple gels Volume of 1 agarose for Number of gels 7x7 cm tray 7x 10 cm tray 1 40 ml 50 ml 2 80 ml 100 ml 4 160 ml 200 ml 8 320 ml 400 ml ii Add the agarose powder to a suitable container e g 500 ml Erlenmeyer flask for 200 ml or less Add the appropriate amount of 1x TAE electropho
40. ash and refilled for the next wash 1 Label the staining trays with your initials and class period You will stain 2 gels per tray 2 Stain gels Remove each gel from the gel tray and carefully slide it into the staining tray Pour approximately 120 ml of 100x stain into the staining tray If necessary add more 100x stain to completely submerge the gels Stain the gels for 2 3 minutes but not for more than 3 minutes Using a funnel pour the 100x stain into a storage bottle and save it for future use The stain can be reused at least 7 times 3 Rinse gels 2 3 minutes Transfer the gels into a large container containing 500 700 ml of clean warm 40 55 C tap water Gently shake the gel in the water for 10 seconds to rinse 10 seconds 36 Student Manual 4 Wash gels Transfer the gel into a large container with 500 700 ml of clean warm tap water Gently rock or shake the gel on a rocking platform for 5 minutes If no rocking platform is available move the gels gently in the water once every minute 5 minutes 5 Wash gels Perform a second wash as in step 4 5 minutes 6 Record results Pour off the water and examine the stained gels for expected DNA bands The bands may appear fuzzy immediately after the second wash but will begin to develop into sharper bands within 5 15 minutes after the second wash This is due to Fast Blast stain molecules migrating into the gel and binding more tightly to the DNA To o
41. at 150 and 43 bp are too small to be observed on the gel Mapping the Plasmid Questions 1 How big is plasmid S5 Add the fragments in each column The total should add up to the size of the plasmid Why The plasmid is 9481 bp in size The fragments are cut from the plasmid and all the pieces together should be equal to the size of the original plasmid 2 Look atthe data from the EcoRI digest of plasmid S5 How many fragments are there Did the enzyme cut the plasmid or did it remain as a circle How could you tell There should be only one fragment At first glance it is not possible to tell if the plasmid was cut although sometimes a circular and possibly twisted plasmid does not run through an agarose gel at the same place as a linear piece of DNA of the same size 3 Compare the data from the Psi digest of plasmid S5 with that of the EcoRI digest How many fragments are there How many restriction sites are there for Psi There should be 7 fragments and therefore 7 restriction sites 4 How many fragments are there when EcoRI and Psil are used to digest plasmid S5 Does that answer the question of whether or not EcoRI cut the plasmid Why There should be 8 fragments when the plasmid is cut by both enzymes The additional fragment shows that EcoRI also cut the plasmid one time 5 Which fragment of Psil digested plasmid S5 was shortened by an EcoRI cut The 2860 bp fragment was cut into two fragments 2817 bp and 43 bp 6
42. ated when plasmid S2 is cut by Pvull Size is calculated by subtracting the site locations from each other Note if a fragment contains the 0 point of the plasmid it is not just a simple subtraction How big are the fragments from plasmid S2 that is cut with Pvull The fragment sizes should add up to the total for that plasmid 5869 base pairs The fragment sizes are 1417 1938 and 2514 bp If the fragments from the plasmid S2 digested with Pvull were run on an agarose gel what would they look like Draw the gel and label the fragments and their sizes 2514 1938 1417 Now you can determine the fragment sizes of the plasmids when cut with the two enzymes EcoRI and Pst Indicate the sizes of the fragments that would be generated if the plasmid were a digest by Psil alone EcoRI alone or by both Psi and EcoRI Plasmid S2 5869 bp l mwa o a 80 7 If plasmid S2 was digested and run on an agarose gel what would the gel look like Draw a gel and the fragment sizes if digested by EcoRI alone Psti alone and by EcoRI and Pstl together 2 EcoRI Pst Both Enzymes Q 5809 a 2860 2817 a 1700 1700 lt 1159 1159 150 150 43 43 8 How does your diagram in question 7 compare to what was observed in your gel after the experiment Indicate a reason for why your data in question 7 might be different from the actual experimental data seen from lesson 2 They should be similar but the bands
43. ation If Pvull was used to cut digest this plasmid how many fragments would it make 4 Next determine the size of the fragments created when plasmid S2 is cut by Pvull DNA fragment size is calculated by subtracting the site locations from each other Note if a fragment contains the 0 point of the plasmid it is not just a simple subtraction How big are the fragments from plasmid S2 that is cut with Pvull The fragment sizes should add up to the total for that plasmid 5869 bp 5 Ifthe fragments from the plasmid S2 digested with Pvull were run on an agarose gel what would they look like Draw the gel and label the fragments and their sizes Student Manual 50 6 Now you can determine the fragment sizes of the plasmids when cut with the two enzymes EcoRI and Psi Indicate the sizes of the fragments that would be generated if the plasmid were a digest by Psti alone EcoRI alone or by both Psi and EcoRI Plasmid S2 5869 bp Fragments gt z s ZO qc 2z O E O W gt H Xx o U 7 If plasmid S2 was digested and run on an agarose gel what would the gel look like Draw a gel and the fragment sizes if digested by EcoRI alone Psti alone and by EcoRI and Psil together 8 How does your diagram in question 7 compare to what was observed in your gel after the experiment Indicate a reason for why your data in question 7 might be different from the actual experimental data seen from lesson 2 Mapping the P
44. bsence of visible evidence of change is it still possible that the DNA samples were fragmented Explain your reasoning Yes They may be chemically changed but the changes may not be visible Enzymes may have cut the DNA 4 After a 24 hour incubation period are there any visible clues that the restriction enzymes may have in some way changed the DNA in any of the tubes Explain your reasoning No No visible change apparent in the tubes but the enzymes may have cut the DNA The reactions are at the molecular level and too small to be seen 73 XIGNAddV Lesson 2 Agarose Gel Electrophoresis Review Questions 1 The electrophoresis apparatus creates an electrical field positive and negative ends of the gel DNA molecules are negatively charged To which pole of the electrophoresis field would you expect DNA to migrate or Explain Positive What color represents the negative pole The negative pole or cathode is black The positive pole or anode is red After DNA samples are loaded in wells they are forced to move through the gel matrix Which size fragment large vs small would you expect to move toward the opposite end of the gel most quickly Explain Smaller There is less resistance to their movement through the gel matrix Which fragments are expected to travel the shortest distance remain closest to the well Explain Larger There is more resistance to their movement through the gel matrix
45. btain maximum contrast additional washes in warm water may be necessary Destain to the desired level but do not wash the gel in water overnight If you cannot complete the destaining in the allocated time you may transfer the gel to 1x Fast Blast stain for overnight staining See Protocol 2 a Place your gel on a light background and record your results by making a diagram as follows Place a clear sheet of plastic sheet or acetate over the gel Witha permanent marker trace the wells and band patterns onto the plastic sheet to make a replica picture of your gel Remove the plastic sheet for later analysis Alternatively gels can be photocopied on a yellow piece of transparent film for optimal contrast b Dry the agarose gel as a permanent record of the experiment i Trim away any unloaded lanes with a knife or razor blade Cut your gel from top to bottom to remove the lanes that you did not load samples into leaving only lanes 1 4 ii Place the gel directly upon the hydrophilic size of a piece of gel support film Water will form beads on the hydrophobic side of a piece of gel support film Center the gel on the film and remove bubbles that may form between the gel and film Place the film on a paper towel and let the gel dry in a well ventilated area making sure to avoid direct exposure to light As the gel dries it will bond to the film but will not shrink If left undisturbed on the support film the gel will dry completely at room
46. c procedures as well as in paternity determinations to discern genetic relationships between individuals at the molecular level This kit allows students to play the role of a forensic scientist and make a positive D that is to simulate using real DNA as evidence and figure out for themselves Who done it In this activity students analyze six different samples of plasmid DNA One sample collected from a hypothetical crime scene and five samples obtained from suspects are digested with two restriction enzymes The resulting DNA fragments are separated and visualized in agarose gels using Bio Rad s Fast Blast DNA staining solution Based on the restriction fragment patterns students compare the evidence and match one of the suspects DNA to the sample collected at the crime scene As an alternative to the classical human forensic applications for this kit have your students imagine they are high tech pathologists investigating an outbreak of an aggressive infectious disease that has never been seen before The Centers for Disease Control and Prevention suspects that a new strain of bacteria has arisen that not only is the cause of the new disease but also has acquired multiple resistance plasmids from some other bacterial strains Their job is to develop a DNA diagnostic tool for identifying the culprit plasmids They decide to use restriction enzyme analysis and DNA electrophoresis fingerprinting to identify and di
47. ces in samples of DNA from different people Student Manual z Za 3 EO z wW O QX pg V Q 23 U J m gt Ww gt O a lt lt TWANVIN LNAGNLS Pre Lab Focus Questions Introduction to DNA Fingerprinting Consideration What is the structure of DNA 1 Compare the backbone of the sugar phosphate arrangement in the side chains of all three figures Are there any differences In the above figure do all three samples contain the same bases Describe your observations Are the bases paired in an identical manner in all three samples Describe the pattern of the base pair bonding In your attempt to analyze DNA samples from three different individuals what conclusions can you make about the similarities and differences of the DNA samples What will you need to compare between these DNA samples to determine if they are identical or non identical Student Manual 24 Lesson 1 Restriction Digestion of DNA Samples Consideration How can we detect differences in base sequences At first sight your task might seem rather difficult You need to determine if the linear base pair sequence in the DNA samples is identical or not An understanding of some historically important discoveries in recombinant DNA technology might help you to develop a plan In 1968 Dr Werner Arber at the University of Basel Switzerland and Dr Hamilton Smith at the Johns Hopkins University Baltimore discovered
48. d the restriction enzyme that recognizes that base sequence is present and digests the DNA how many DNA fragments will be produced 5 9 If the GAATTC palindrome repeats are randomly spaced along the DNA strand then what can you say about the size of the fragments that will be produced when the DNA is digested with a restriction enzyme that recognizes that sequence Random sized fragments will be produced 86 Applying What You Have Learned 1 Ifa DNA molecule has two restriction sites for restriction enzyme A how many fragments would be produced if the DNA is cut by enzyme A A A l b Number each fragment 1 A 2 A Which fragment would be the largest Fragment 3 Which fragment would be the smallest Fragment 2 Draw a DNA molecule that has five randomly spaced restriction sites for a specific palindrome How many fragments would be produced if they were each cut by a restriction enzyme 6 Label each fragment Answers will vary Rank them in order of size from largest to smallest Answers will vary A l B In this diagram A and B are different palindrome sequences on a DNA strand Only the restriction enzyme that recognizes site B is present 8 Explain why only two fragments would be produced The enzyme would cut only at site B producing two DNA fragments 87 APPENDIX C XIGNAddV Prelab Activity 2 A Review of Electrophoresis from Appendix B A piece of DNA is cut int
49. d DNA to other bacteria via conjugation Scientists routinely take advantage of plasmid DNA because its small size makes it easy to purify and once a genetically engineered DNA sequence has been added it can be reintroduced into bacterial cells using a procedure called transformation Plasmids cut with a restriction enzyme can be joined to foreign DNA from any source that has been cut with the same enzyme The resulting hybrid DNA can then be transformed into bacterial cells The hybrid plasmids can perpetuate themselves in bacteria just as before except that the foreign DNA that was joined to them is also perpetuated Every hybrid plasmid now contains a copy of the piece of foreign DNA joined to it We say that the foreign piece of DNA has been cloned and the plasmid DNA that carried it is called a vector During this hybrid plasmid construction process it is necessary to confirm that the foreign DNA has been successfully inserted into the host plasmid While it is possible to have the complete DNA sequence of each construct determined it is easier and quicker to use a restriction digestion to create a plasmid map Plasmids can be mapped described in terms of the location of restriction sites using simple experiments and the use of logic The general procedure is to digest a plasmid with two restriction enzymes separately two single digests and then together a double digest Sizes of fragments are then estimated by comparison with
50. d by DNA base pairs of sites where the plasmid may be cut by particular restriction enzymes The name of the plasmid and its size of DNA in bp is shown inside the circle In addition it shows the Origin of Replication Ori the gene encoding beta lactamase the enzyme that gives the bacteria resistance to the antibiotic ampicillin and the location where foreign DNA from the lambda bacteriophage was inserted Refer to the plasmid maps on page 49 for more detail 48 Student Manual Sample Plasmid Maps Pyull 55 EcoRI 255 BamHI 276 Pstl 298 gt z s ZO qc 2z O oe Ow gt H Xx o U Scal 4375 Pyull 1993 PstI 1998 Pst 2148 Pyull 3410 Scal 2336 Hind 3315 Psl 3307 Plasmid S2 Pvull 55 EcoRI 255 BamHI 276 Psfl 298 Pstl 370 Scal 7987 Psfl 2356 Psfl 2520 Pvull 7022 HindIII 6927 Pst 6919 BamHI 6624 Pst 6451 EcoRV 3309 Pstl 3613 EcoRV 5450 EcoRV 4047 Pyull 4300 Plasmid S5 Student Manual 49 TWANVIN LNAGNLS m gt X lt m Z 2 O gt O lt ok Reading a Plasmid Map Questions 1 From the map of plasmid S2 list all the restriction enzymes that would cut this plasmid 2 Which plasmid S2 or S5 is the biggest and what is its size 3 Using plasmid S2 as an example find the restriction sites for the enzyme Pvull How many sites are there What is their loc
51. e recognition sites in the plasmids by use of logic Plasmid mapping has revolutionized molecular biology and paved the way for the biotechnology industry This technique allows molecular biologists to quickly evaluate the success of cloning experiments as well as to easily identify plasmids and associated traits in different organisms Although real world DNA fingerprinting is performed on genomic DNA this activity utilizes plasmid DNA to simulate how real DNA fingerprints are analyzed Plasmids are circular non chromosomal pieces of DNA that can replicate in bacteria Plasmids often carry genes encoding resistance to antibiotics which gives bacteria a selective advantage over their competitors a gt z s ZO qc z O oe Ow gt H Xx oO U Scientists routinely take advantage of plasmid DNA and a natural bacterial defense mechanism the restriction enzyme as the basis for much of biotechnology Restriction enzymes allow bacteria to destroy DNA from invading bacteriophages phages which are viruses that infect and destroy bacteria Restriction enzymes recognize specific DNA sequences within the phage DNA and then cut the DNA at that site Fragmented DNA no longer poses a threat to bacterial survival Purified restriction enzymes can be used in the laboratory to cut DNA isolated from any organism not just phage DNA After plasmids are cut with a restriction enzyme they can be joined or ligated to a piece of DNA fro
52. e resulting fragments can then be used to create a plasmid map see page 47 Instructor s Manual Agarose Gel Electrophoresis Agarose gel electrophoresis separates DNA fragments by size DNA fragments are loaded into an agarose gel slab which is placed into a chamber filled with a conductive buffer solution A direct current is passed between wire electrodes at each end of the chamber Since DNA fragments are negatively charged they will be drawn toward the positive pole anode when placed in an electric field The matrix of the agarose gel acts as a molecular sieve through which smaller DNA fragments can move more easily than larger ones Therefore the rate at which a DNA fragment migrates through the gel is inversely proportional to its size in base pairs Over a period of time smaller DNA fragments will travel farther than larger ones Fragments of the same size stay together and migrate in single bands of DNA These bands will be seen in the gel after the DNA is stained Consider this analogy Imagine that all the desks and chairs in the classroom have been randomly pushed together An individual student can wind his her way through the maze quickly and with little difficulty whereas a string of four students would require more time and have difficulty working their way through the maze DNA Fingerprinting Each person has similarities and differences in DNA sequences To show that a piece of DNA contains a specific nucleotide sequence
53. ecial sequence of bases on the DNA called restriction sites A restriction endonuclease cuts two DNA molecules at the same location What can you assume is identical about the molecules at that location The restriction sites are identical Do any of your suspect samples appear to have EcoRI or Psil recognition sites at the same location as the DNA from the crime scene The samples in lanes 2 and 5 match CS and S3 Based on the above analysis do any of the suspect samples of DNA seem to be from the same individual as the DNA from the crime scene Describe the scientific evidence that supports your conclusion The CS and S3 samples appear to be identical They both produce similar banding patterns on the gel 79 XIGNAddV Extension Activity 1 Plasmid Mapping Reading a plasmid map 1 From the map of plasmid S2 list all the restriction enzymes would cut this plasmid Pvull EcoRI BamHI Psi EcoRV Hindlll Scal Which plasmid S2 or S5 is the biggest and what is its size S5 is the largest 9481 bp Using plasmid S2 as an example find the restriction sites for the enzyme Pvull How many sites are there What is their location If Pvull was used to cut digest this plasmid how many fragments would it make There are three sites for Pvull on plasmid S2 They are at position 55 1993 and 3410 Three fragments would be created if plasmid S2 was digested with Pvull Next determine the size of the fragments cre
54. el support film Center the gel on the film on a paper towel and let the gel dry in a well ventilated area making sure to avoid direct exposure to light As the gel dries it will bond to the film but will not shrink If left undisturbed on the support film the gel will dry completely at room temperature after 2 3 days The result will be a flat transparent and durable record for the experiment Gel support film Note Avoid extended exposure of dried gels to direct light to prevent band fading However DNA bands will reappear if the dried gels are stored in the dark for 2 3 weeks after fading l lt Z lt Z Lu a H 2 N Z O V e9 W j Student Manual 39 Post Lab Thought Questions 1 What can you assume is contained within each band 2 If this were a fingerprinting gel how many samples of DNA can you assume were placed in each separate well 3 What would be a logical explanation as to why there is more than one band of DNA for each of the samples 4 What caused the DNA to become fragmented 5 Which of the DNA samples have the same number of restriction sites for the restriction endonucleases used Write the lane numbers 6 Which sample has the smallest DNA fragment 7 Assuming a circular piece of DNA plasmid was used as starting material how many restriction sites were there in lane three 8 From the gel drawing on page 35 which DNA samples appea
55. ently tap on the table top Using a separate tip for each sample add 5 ul of loading dye LD into each tube Cap the tubes and mix by gently flicking the tube with your finger Collect the sample at the bottom of the tube by tapping it gently on the table or by pulse spinning in a centrifuge Remove the agarose gel from the refrigerator if applicable and remove the plastic wrap Place the agarose gel in the electrophoresis apparatus Fill the electrophoresis chamber with 1x TAE buffer to cover the gel using approximately 275 ml of buffer for a Bio Rad Mini Sub Cell horizontal electrophoresis chamber Check that the wells of the agarose gels are near the black electrode and the bottom edge of the gel is near the red electrode Using a separate tip for each sample load the indicated volume of each sample into 7 wells of the gel in the following order Lane 1 M DNA size marker 10 ul Lane 2 CS green tube 20 ul Lane 3 S1 blue tube 20 ul Lane 4 S2 orange tube 20 ul Lane 5 S3 violet tube 20 ul Lane 6 S4 red tube 20 ul Lane 7 S5 yellow tube 20 ul Carefully place the lid on the electrophoresis chamber The lid will attach to the base in only one orientation The red and black jacks on the lid of the horizontal electrophoresis chambers will match with the red and black jacks on the base Plug the electrodes into the power supply red to red and black to black Turn o
56. ere used together in a double digest The resulting fragments were run on a gel to solve the who done it The background material can be used to construct a plasmid map Since the plasmids are circular the number of fragments represents the number of cuts or restriction sites To visualize this take a rubber band and cut it once How many frag ments are there Cut the same rubber band again How many fragments are there now The most informative part of plasmid mapping comes from using logic to overlap the infor mation from two single digests with information obtained from a double digest How do the cuts from one restriction enzyme overlay with cuts from a second restriction enzyme There are clues to see how to overlap them Do any of the first fragments remain uncut Student Manual 47 TWANVIN LNAGNLS m gt X lt m Z 2 O a gt O lt ok with the second enzyme Do the sizes of any of fragments from the double digest add up the size of a fragment from a single digest Do any of the fragments seem to remain the same size after being cut by the second enzyme A simple example is shown below 1000 bp plasmid example DNA size Digested with Digested with Digested with marker Undigested Enzyme 1 Enzyme 2 Enzyme 1 amp 2 1000 bp 1000bp 1000 bp 700 bp 700 bp 500 bp 500 bp 300 bp 300 bp 300 bp 200 bp 200 bp 700 500 300 300 Note that the two 1000 bp fragments undigested
57. es Advance Preparation Objectives Rehydrate DNA buffer samples and restriction enzymes Aliquot restriction enzymes Pour agarose gels to prepare for lesson 2 If you prefer to have your students pour their own gels during the lab prepare the molten agarose ahead of time If prepared in advance molten agarose should be kept in a water bath set at 50 55 C until gels are poured Set temperature of 37 C for water bath or incubator Set up student and instructor workstations Time required Thirty minutes to 1 hour depending on how you choose to prepare agarose gels What s required Horizontal electrophoresis gel chamber casting trays and combs Electrophoresis buffer 50x TAE Agarose powder 8 clear microtubes 3 liters distilled water Procedures 3 Note All of the DNA and enzyme vials should contain a white residue which may appear as a loose powder in the DNA vials The lyophilized DNA samples have color coded labels on clear glass vials The lyophilized EcoRI Psil enzyme mix is in an amber vial Rehydrate DNA samples A To rehydrate DNA samples carefully remove the stopper and add 200 ul of sterile water to each lyophilized DNA vial Replace the stopper and vigorously shake the vial It is critical to dissolve all the powder some of which may be stuck to the stop per Allow DNA buffer samples to rehydrate at room temperature for 15 minutes or until dissolved Gentle heating at 37 C for 10 minutes may be nece
58. est How many fragments are there How many restriction sites are there for Psi How many fragments are there when EcoRI and Psi are used to digest plasmid S5 Does that answer the question of whether or not EcoRI cut the plasmid Why gt a2 s ZO q 2z O g2 O W 2 H Xx oO W Which fragment of Psi digested plasmid S5 was shortened by a cut with EcoRI How do you know this Draw the Psti fragment that is cut with EcoRI in plasmid S5 to demonstrate how the fragment was cut with EcoRI Plasmid S3 7367 bp Fragments 6504 863 moa Restriction mapping is an exercise in critical thinking and logic Plasmid S5 is difficult to completely map because of the numerous Pst restriction sites With the data it would be very difficult to place all the restriction sites in order It is easier to map plasmid S3 Shown above is the data generated from digestion of plasmid S3 with EcoRI and Pst How many times did EcoRI cut plasmid S3 What are the fragment sizes Student Manual 53 8 The data from the EcoRI digest of plasmid S3 indicate that the fragments are not equal Draw a possible map and label the EcoRI sites and the sizes of the fragments TWANVIN LNAGNLS m gt lt j m Z 2 O Z gt O lt 9 Now draw an approximate map of the Pst sites on plasmid S3 and label the Psti sites and the sizes of the fragments 10 Draw a circular map of plasmid S3 digested with both Pstl and EcoR
59. f experimental controls Interpretation of experimental results Use of DNA evidence in court Creation and use of standard curves Environmental and Health Science Epidemiology and disease Genetic testing Role place limits and possibilities of science and technology Privacy of information issues Chemistry of Life DNA structure function and chemistry e Cell structure and organization Ilan e Chemistry of DNA e Tissue types for biological Cell and electrophoresis Molecular Biochemistry of sampling e Plasmid mapping restriction enzymes Biology Genetic variations in the human genome Genotype vs phenotype e Restriction fragment length polymorphisms RFLP analysis e Biodiversity e Genetic engineering techniques Bacterial defense e Mendelian inheritance mechanisms e Plasmid mapping Table of Contents Overview Kit Inventory Checklist Kit Components and Required Accessories 2 Instructors Manual casisssissicussaviesasiessencntetecetasacucsetedacvdncesicusissane 4 Instructors Manual Background Setting the Stage for Your Students c00 4 Instructor s Advance Preparation Guide cscesesseeeeeseeeseneees 9 Implementation Timeline Advance Preparation and Student Lessons 9 Workstation Checklist Student and Instructor Lab Setups ccee 11 Instructors Advance Preparation Lab Prep and Lesson Highlight
60. ferently Can one predict fragment sizes using plasmid maps constructed from the lambda bacteriophage genome In this activity you will design a new plasmid The parent plasmid pTZ18U used for plasmid construction is 2860 bp in size It has numerous restriction sites see diagram on pages 56 57 The five plasmids constructed for the DNA fingerprinting lab were all based on this plasmid The pTZ18U plasmid was digested with the Psi restriction enzyme Lambda phage DNA was also digested with the Psi restriction enzyme and the resulting fragments were then inserted into the Psi digested pTZ18U plasmid As you look at the different plasmids notice that each plasmid contains different fragments of lambda phage DNA For example plasmid S1 contains lambda sequence 20285 22425 Student Manual 55 N gt E a 5 20 qc z O a2 SE H Xx V Wi Pyull 55 EcoRI 255 BamHI 276 Psil 298 BamHI 369 EcoRV 1448 Scal 3506 EcoRI 1489 Pvull 2022 TWANVIN LNAGNLS Pst 2438 Pvull 2541 rindi 2446 m gt lt m Z 2 O gt O lt N Plasmid S1 Pyull 55 EcoRI 255 BamHI 276 Pstl 298 BamHI 585 Pstl 766 Scal 5765 EcoRV 1763 Pyull 4800 HindIII 4705 Pstl 4697 Pyull 2913 EcoRV 3166 EcoRV 3904 Pstl 3604 Plasmid S4 Student Manual 56 Pyull 55 EcoRI 255 BamHI 276 Pstl 298 HindIII 306 Pvull
61. from any source Restriction enzymes were named before scientists understood how they functioned because they would limit or restrict the growth of phages A restriction enzyme sits ona DNA molecule and slides along the helix until it recognizes specific sequences of base pairs that signal the enzyme to stop sliding The enzyme then cuts or chemically separates the DNA molecule at that site called a restriction site If a specific restriction site occurs in more than one location on a DNA molecule a restriction enzyme will make a cut at each of those sites resulting in multiple fragments Therefore if a linear piece of DNA is cut with a restriction enzyme whose specific recognition site is found at two different locations on the DNA molecule the result will be three fragments of different lengths If the piece of DNA is circular and is cut with a restriction enzyme whose specific recognition site is found at two different locations on the DNA molecule the result will be two fragments of different lengths The length of each fragment will depend upon the location of restriction sites on the DNA molecule When restriction enzymes are used to cut strands of circular plasmid DNA such as the samples included in this kit fragments of varying sizes are produced DNA that has been cut with restriction enzymes can be separated and observed using a process known as agarose gel electrophoresis The term electrophoresis means to carry with electricity Th
62. g tray on a rocking platform and agitate overnight If no rocking platform is available agitate the gels staining tray a few times during the staining period You should begin to see DNA bands after 2 hours but at least 8 hours of staining is recommended for complete visibility of stained bands Stain overnight It is crucial that you shake gels gently and intermittently while performing the overnight staining in 1x Fast Blast stain since smaller fragments tend to diffuse without shaking 38 Student Manual 3 Record results No destaining is required after staining with 1x Fast Blast The gels can be analyzed immediately after staining a Place your gel on a light background and record your results by making a diagram as follows Place a clear sheet of plastic sheet or acetate over the gel With a permanent marker trace the wells and band patterns onto the plastic sheet to make a replica picture of your gel Remove the plastic sheet for later analysis Alternatively gels can be photocopied on a yellow piece of transparent film for optimal contrast b Dry the agarose gel as a permanent record of the experiment i Trim away any unloaded lanes with a knife or razor blade Cut your gel from top to bottom to remove the lanes that you did not load samples into leaving only lanes 1 4 ii Place the gel directly upon the hydrophilic size of a piece of gel support film Water will form beads on the hydrophobic side of a piece of g
63. h shorter time In this lab activity students will compare band patterns produced by restriction enzyme cleavage of DNA samples when separated on an agarose gel RFLP The patterns in this exercise are produced from one sample that represents DNA taken at the crime scene and five samples obtained from suspects in the case It may be important for you to point out to your students that this laboratory exercise models the more elaborate technique that is performed on complex human DNA samples Restriction Enzymes Scientists have benefited from a natural bacterial defense mechanism the restriction enzyme A restriction enzyme acts like molecular scissors making cuts at specific sequence of base pairs that it recognizes These enzymes destroy DNA from invading viruses or bacteriophages phages Phages are viruses that infect and destroy bacteria Bacterial restriction enzymes recognize very specific DNA sequences within the phage DNA and then cut the DNA at that site Although the bacteria s own DNA may also contain these sites the bacteria protect their own restriction sites by adding a methyl group Once purified in the laboratory the fragmented phage DNA no longer poses a threat to the bacteria These restriction endonucleases endo within nuclease enzyme that cuts nucleic acids are named for the bacteria from which they were isolated For example EcoRI was isolated from Escherichia coli Restriction enzymes can be used to cut DNA isolated
64. he greater number of base pairs be located toward the top of the gel or the bottom Why 2 Suppose you had 500 pieces of each of the four fragments how would the gel appear 3 If it were possible to weigh each of the fragments which one would be the heaviest Why 4 Complete this rule for the movement of DNA fragments through an agarose gel The larger the DNA fragment the 68 This diagram represents a piece of DNA cut with Hindlll at each of the restriction sites pointed to by the arrows The numbers represent the number of base pairs in each fragment 23 130 ead a i 9 416 aig 6 557 4 361 5 How many fragments were produced by the restriction enzyme Hindlll 6 On the gel diagram show how you believe these fragments will sort out during electrophoresis The two fragments with no length indicated will be too small to be visualized on the gel Well Negative Positive 7 Label each fragment with its correct number of base pairs APPENDIX B 69 XIGNAddV Appendix C Instructor s Answer Guide Pre Lab Focus Questions Introduction to DNA Fingerprinting 1 Compare the backbone of sugar phosphate arrangement in the side chains of all three figures Are there any differences The arrangement is identical for all three samples In the above figure do all three samples contain the same bases Describe your observations All samples contain the same bases adenine thymine g
65. he leveling bubble provided with the chamber iii Prepare the desired concentration and amount of agarose in 1x TAE electrophoresis buffer iv Cool the agarose to at least 60 C before pouring v While the agarose is cooling to 60 C place the comb into the appropriate slot of the gel tray Gel combs should be placed within 1 2 inch of the end of the gel casting tray if a single well 7 x 7 cm gel is cast To pour a double well gel using a 7 x 10 cm tray and two 8 well combs place one comb at one end of the tray and the other comb in the middle of the tray The combs will form the wells into which the samples will be loaded vi Allow the gel to solidify at room temperature for 10 to 20 minutes It will appear cloudy or opaque when ready to use vii Carefully remove the comb from the solidified gel viii Remove the tape from the edges of the gel tray ix You have two options JZ a9 Zq Sg o co Oo OO a2 a es vA Za Option 1 If you do not have sufficient time to proceed to Lesson 2 store gels ina sealable plastic bag with 1 2 ml of 1x TAE running buffer at room temperature for 1 day or in the refrigerator 4 C for up to 1 week before using Have your students label their plastic bags Option 2 If there is sufficient time to proceed to Lesson 2 place the tray onto the leveled DNA electrophoresis chamber so that the sample wells are at the black cathode end of the base DNA samples will migrate towards t
66. he red anode end of the chamber during electrophoresis Restriction Digests A 45 minute incubation at 37 C is the optimum digestion condition If a 37 C heating block water bath or incubator is not available samples can be digested by placing tubes in foam micro test tube holders floating them in a large volume 1 liter or more of 37 C water and allowing them to incubate overnight as the water cools to room temperature Instructor s Manual 15 Practice Using Micropipets Optional We recommend that you familiarize your students with proper pipeting techniques prior to Lesson 1 Have your students learn how to transfer different volumes of a solu tion from one tube into another with a micropipet Students may practice by using either sample loading dye or food coloring mixed with either a dense saturated sugar or glycerol solution Here is a quick summary on how to use micropipets Look at the micropipet to determine the volume range Twist the dial on the micropipet to set the desired volume Attach a clean pipet tip Press the micropipet plunger to the first soft stop Insert the pipet tip into the solution to be transferred Slowly release the plunger to retrieve the liquid Insert the pipet tip into the desired tube D NOTON Press the plunger past the first stop to the second hard stop to transfer the liquid Make sure to keep the plunger pressed when lifting the pipet tip out of the tube 9 Eject the pipet tip
67. his sections outlines the recommended schedule for advanced preparation on the part of the instructor A detailed Advance Preparation Guide is provided on pages 13 19 Activity When Time required Read manual Immediately 1 hour Prepare electrophoresis TAE Prior to or during Lesson 2 1 hour buffer and pour agarose gels Rehydrate lyophilized DNA Prior to Lesson 2 20 minutes buffer samples and enzyme mix and aliquot Prepare Fast Blast Prior to Lesson 3 20 minutes DNA stain Prepare Hindili standard Aliquot loading dye and prepared standard Set up workstations The day of student labs 10 minutes day TWANVIN S HOLONYLSNI gt z S Z 6 m v D a D gt O Z Instructors Manual 10 Workstation Checklist Student Workstations Materials and supplies that should be present at each student workstation prior to beginning each laboratory experiment are listed below The components provided in this kit are sufficient for 8 student workstations we recommend 2 4 students per workstation Teacher s Common Workstation A list of materials supplies and equipment that should be present at a common location which can be accessed by all student groups is also listed below It is up to the discretion of the teacher as to whether students should access common buffer solutions and equipment or whether the teacher should aliquot solutions and operate equipment To avoid the potential for contamination and spills you
68. hould be worn to avoid staining clothes Dispose of the staining solutions according to protocols at your facility Use either 10 bleach solution or a 70 alcohol solution to remove Fast Blast from most surfaces Verify that these solutions do not harm the surface prior to use Note e We recommend using 120 ml of diluted Fast Blast to stain two 7 x 7 cm or 7 x 10 cm agarose gels in individual staining trays provided in the kit you may want to notch gel corners for identification If alternative staining trays are used add a sufficient volume of staining solution to completely submerge the gels e Following electrophoresis agarose gels must be removed from their gel trays before being placed in the staining solution This is easily accomplished by holding the base of the gel tray in one hand and gently pushing out the gel with the thumb of the other hand e Because the gel is fragile special attention must be given when handling it We highly recommend using a large spatula or other supportive surface to transfer the gel from one container to another during the destaining steps involved with the quick staining protocol e Destaining when performing the quick staining protocol requires the use of at least one large volume container capable of holding at least 500 ml at each student workstation Each student team may utilize separate washing containers for each wash step or simply use a single container that is emptied after each wash a
69. in a 1 agarose gel while the xylene cyanol the slower dye comigrates with DNA fragments of approximately 4 000 bp ina 1 agarose gel Staining the DNA pinpoints its location on the gel When the gel is immersed in Fast Blast DNA stain the stain molecules attach to the DNA trapped in the agarose gel When the bands are visible your students can compare the DNA restriction patterns of the different samples of DNA The gel on page 7 shows the DNA pattern that will be obtained by your students following electrophoresis The DNA from the crime scene has been labeled CS that from Suspect 1 S1 and so on The DNA from the crime scene is placed in lane 2 one suspect s DNA is placed in each of lanes 3 4 5 6 and 7 Lane 1 contains Hindlll lambda digest DNA size markers By convention the lanes are numbered from the top left The students task is to look at the DNA banding patterns and see if any of the suspects bands match those of the DNA found at the crime scene Instructor s Manual M CS S1 S2 S3 S4 S 1 2 3 4 5 6 7 8 anra E ie i l lM font E fe a m ve a It is easy to see that the DNA taken from the crime scene and the DNA from S3 are identical You may want to point out how strong or weak this evidence is in convicting a suspect The DNA evidence may place the suspect at the scene but other evidence may be needed to prove him or her guilty You may point out to your student
70. iology conservation biology and biotechnology Have your students research a scenario that is interesting to them and present their findings to the class 1 Food identification endangered species identification The purity or impurity of ground beef has been proven using DNA typing Hamburger has been shown to often be a mixture of pork and other non beef meats Using portable testing equipment authorities have used DNA typing to determine that the fish served in sushi was really meat from whales and dolphins These are many times endangered species that are protected by international law 2 Accused and convicted felons set free because of DNA typing A man imprisoned for 10 years was released when DNA testing unavailable when he was convicted was used to show that he could not have been the rapist Statistics show that about 1 3 of all sexual assault suspects are freed as a result of DNA testing 3 Identifying human remains Scientists have used DNA typing to confirm that the body in the grave was or was not the person that was supposed to be there Bones found in Russia are believed to be those of the Romanovs Russia s last imperial family Czar Nicholas II and his family were executed by the Bolsheviks in 1918 Experts from around the world have been studying the bones to match skulls teeth and other features with photographs DNA from the bones was compared to that of known descendants and it was determined that the bone
71. lasmid The first step in mapping a plasmid is to determine how many times a restriction site is found on that plasmid First examine the results for plasmid S5 as an example The data given in the following table are for the double digest using both Ecol and Psil Also given are the data for single digests by the individual enzymes The numbers in the columns under each enzyme represent the sizes of all of the fragments that are formed when each enzyme is used for a single digest The charts below show the sizes of fragments that will be generated when plasmid S5 has been digested with the indicated restriction enzyme Student Manual 51 Pvull 55 EcoRI 255 TWANVIN LNAGNLS m gt X lt m Z 2 O a gt O lt ok Scal 7987 Psfl 2356 Pstl 2520 Pvull 7022 Hindill 6927 Pst 6919 BamHI 6624 Pst 6451 EcoRV 3309 Pstl 3613 EcoRV 5450 EcoRV 4047 Pvull 4300 Plasmid S5 Plasmid S5 9481 bp Enzymes EcoRI Psi Both l O A Mapping the Plasmid Questions 1 How big is plasmid S5 Add the fragments in each column The total should add up to the size of the plasmid Why 2 Look at the data from the EcoRI digest of plasmid S5 How many fragments are there Did the enzyme cut the plasmid or did it remain as a circle How could you tell Student Manual 52 Compare the data from the Psi digest of plasmid S5 with that of the EcoRI dig
72. m any organism foreign DNA that has been cut with the same enzyme The resulting hybrid DNA plasmid can be put into transformed bacterial cells A hybrid plasmid can replicate itself in bacteria similar to the original plasmid except that the foreign DNA that was incorporated is also perpetuated Every hybrid plasmid now contains a copy of the piece of foreign DNA joined to it We say that the foreign piece of DNA has been cloned and the plasmid DNA that carries it is called a vector The crime scene and suspect DNA samples in this kit were created by inserting lambda phage DNA that had been digested with the Pst restriction enzyme into Pstl digested plasmid pTZ18U Recombinant plasmids were selected that gave distinct striking banding patterns or restriction fragment length polymorphisms RFLP when digested with restriction enzymes Psti and EcoRI and analyzed on an agarose gel Restriction maps of some of the crime scene and suspect plasmids are included on page 48 Plasmids can be mapped or described in terms of location of restriction sites using simple experiments and logic The general procedure is to cut digest a plasmid with two restriction enzymes separately two single digests and the together a double digest Sizes of the resulting DNA fragments are determined then one uses logic to determine the relative location of the restriction sites In the forensic DNA fingerprinting lab two restriction enzymes Psti and EcoRI w
73. may choose to aliquot stock solutions of DNA and enzymes for the students All other reagents should be kept at az the front of the room for student teams to access as they need them 2 Z Lesson 1 Restriction Digestion of DNA Samples g c Materials Needed for Each Workstation Quantity v o m Agarose gel electrophoresis system electrophoresis 1 m co chamber casting tray 8 well comb 2 a EcoRI Psti enzyme mix 1 tube 80 ul m O T Pipet tips 2 200 pl 15 tips Q T Z Adjustable micropipet 2 20 ul 1 m Colored micro test tubes 2 o green blue orange violet red yellow 1 m Permanent marker 1 m Waste container 1 Q Foam micro test tube holder 1 m Laboratory tape not 3M Scotch brand or similar tape 1 Q Instructor s Workstation Crime scene C5 DNA with buffer rehydrated 1 vial Q Suspect 1 S1 DNA with buffer rehydrated 1 vial Q Suspect 2 S2 DNA with buffer rehydrated 1 vial Q Suspect 3 S3 DNA with buffer rehydrated 1 vial m Suspect 4 S4 DNA with buffer rehydrated 1 vial Q Suspect 5 S5 DNA with buffer rehydrated 1 vial Q Molten 1 agarose in 1x TAE See Advance Prep page 14 40 50 ml per gel m 37 C water bath or incubator optional 1 per class Q Microcentrifuge 1 per class O or mini centrifuge 4 per class m Protective eye goggles should be worn in the laboratory at all times Proper safety precautions such as no eating or drinking should always be practiced Instructors Manual 11 TWANV
74. n and need to refer to the lambda bacteriophage genome map that includes the EcoRI sites You must make a plasmid that is at least 5 000 base pairs but not more than 10 000 base pairs in size Remember that the parent plasmid is 2 860 bp in size Where is the EcoRI site on the parent pTZ18U plasmid The EcoRI site is at 255 bp Choose a segment of lambda bacteriophage genome that could be cut out by the EcoRI enzyme Which segment will you use There are three possibilities lambda 21 226 26 104 lambda 26 104 31 747 lambda 39 168 44 972 All other options would make the plasmid larger than 10 000 bp Draw your new plasmid with the insert of your choice Be sure to include the restriction sites for Psil and EcoRI in your drawing How big is your new plasmid Give the positions of the restriction sites in your new plasmid a number indicating the location Remember that the first EcoRI site will still be position 255 as it is in the parent pTZ18U plasmid map POSSIBILITY 1 POSSIBILITY 2 POSSIBILITY 3 Ps EcoRI Lambda 21 226 26 104 4 878 bp insert 7 738 bp total EcoEIl 255 5 133 Pst 1 454 5 176 EcoRI Pst Lambda 26 104 31 747 5 643 bp insert 8 503 bp total EcoRI 255 5 898 Pst 1 083 5 943 EcoRI Pst EcoRI Pst 84 Lambda 39 168 44 972 5 804 bp insert 8664 bp total EcoRI 255 5 059 Pstl 6 102 EcoRI Pst EcoRI 8 664 How many restriction sites are there now for Psi in your new plasmid
75. n the power and electrophorese your samples at 100 V for 30 minutes or 0 25x TAE if using the Fast Gel Protocol DNA Loading Dye lt gS 2em E Centrifuge T R D se QUICK GUIDE Student Manual AGINS AINO Visualization of DNA Fragments 1 When the electrophoresis run is complete turn off the power and remove the top of KY the chamber Carefully remove the gel and y tray from the gel box Be careful the gel RY is very slippery Slide the gel into the staining tray 2 You have two options for staining your gel Quick staining requires 12 15 minutes a Add 120 ml of 100x Fast Blast DNA stain into a staining tray 2 gels per tray b Stain the gels for 2 minutes with gentle agitation Save the used stain for future use c Transfer the gels into a large washing container and rinse with warm 40 55 C tap water for approximately 10 seconds d Destain by washing twice in warm tap water for 5 minutes each with gentle shaking for best results e Record results yy f Trim away any unloaded lanes 4 g Air dry the gel on gel support film and tape the dried gel into your laboratory notebook Overnight staining a Add 120 ml of 1x Fast Blast DNA stain to the staining tray 2 gels per tray b Let the gels stain overnight with gentle shaking for best results No destaining is required c Pour
76. nd refilled for the next wash e 100x Fast Blast can be reused at least seven times e No washing or destaining is required when using the overnight staining protocol Instructor s Manual 18 To obtain a permanent record of the gel before it is dried either trace the gel outline including wells and DNA bands on a piece of paper or acetate take a photograph with a digital camera photocopy the gel or scan the gel Drying the Agarose Gel as a Permanent Record of the Experiment Note Drying agarose gels requires the use of Bio Rad s specially formulated high strength analytical grade agarose Other gel media may not be appropriate for this purpose We recommend using Bio Rad s exclusive gel support film catalog 170 2984EDU to dry agarose gels Remove the stained agarose gel from its staining tray and trim away any unloaded lanes with a knife or razor blade Place the gel directly upon the hydrophilic side of a piece of gel support film Water will form beads on the hydrophobic side but will spread flat on the hydrophilic side of the film Center the gel on the film and remove bubbles that may form between the gel and film Place the film on a paper towel and let the gel dry making sure to avoid direct exposure to light As the gel dries it will bond to the film but will not shrink If left undisturbed on the support film the gel will dry completely at room temperature after 2 3 days The result will be a flat transparent and d
77. nogenic latex or vinyl gloves should be worn while handling the stain or stained gels to keep hands from becoming stained blue Lab coats or other protective clothing should be worn to avoid staining clothes Protocol 1 Quick Staining of Agarose Gels in 100x Fast Blast DNA Stain This protocol allows quick visualization of DNA bands in agarose gels within 15 minutes For quick staining Fast Blast DNA stain 500x should be diluted to a 100x concentration We recommend using 120 ml of 100x Fast Blast to stain two 7 x 7 cm or 7 x 10 cm agarose gels in individual staining trays provided in Bio Rad s education kits If alternative staining trays are used add a sufficient volume of staining solution to completely submerge the gels Following electrophoresis agarose gels must be removed from their gel trays before being placed in the staining solution This is easily accomplished by holding the base of the gel tray in one hand and gently pushing out the gel with the thumb of the other hand Because the gel is fragile special attention must be given when handling it We highly recommend using a large spatula or other supportive surface to transfer the gel from one container to another Destaining requires the use of at least one large volume container capable of holding at least 500 ml at each student workstation Each student team may utilize separate washing containers for each wash step or simply use a single container that is emptied after each w
78. o four fragments as shown in the diagram i A solution of the four fragments is placed in a well in an agarose gel Using the information given above draw on the diagram how you think the fragments might be separated Label each fragment with its corresponding letter Well lt _ Agarose gel Positive Have your teacher check your diagram before you proceed 1 Where would the larger fragments those with the greater number of base pairs be located toward the top of the gel or the bottom Why The large fragments would be towards the top of the gel because it is more difficult for the larger pieces to be strained through the gel 2 Suppose you had 500 pieces of each of the four fragments how would the gel appear There would still be only 4 bands present 3 If it were possible to weigh each of the fragments which one would be the heaviest Why Fragment D would be heaviest because it is the largest piece of DNA and would thus have the greatest mass 4 Complete this rule for the movement of DNA fragments through an agarose gel The larger the DNA fragment the slower it migrates through an agarose gel 88 This diagram represents a piece of DNA cut with Hindlll at each of the restriction sites pointed to by the arrows The numbers represent the number of base pairs in each fragment 23 130 a o it 9 416 i I 6 557 5 How many fragments were produced by the restriction enzyme Hindlll APPENDIX C
79. or represents the negative pole 3 After DNA samples are loaded into the sample wells they are forced to move through the gel matrix What size fragments large vs small would you expect to move toward the opposite end of the gel most quickly Explain m N oe O Z N n Cc g m Z gt Z Cc gt 4 Which fragments large vs small are expected to travel the shortest distance from the well Explain Student Manual 34 Staining DNA with Fast Blast DNA Stain Laboratory Procedure Consideration Are any of the DNA samples from the suspects the same as that of the individual at the crime scene Take a moment to think about how you will perform the analysis of your gel In the final two steps you will A Visualize DNA fragments in your gel B Analyze the number and positions of visible DNA bands on your gel Making DNA Fragments Visible Since DNA is naturally colorless it is not immediately visible in the gel Unaided visual examination of the gel after electrophoresis indicates only the positions of the loading dyes and not the positions of the DNA fragments DNA fragments are visualized by staining the gel with a blue stain called Fast Blast DNA stain The blue stain molecules are positively charged and have a high affinity for the DNA These blue stain molecules strongly bind to the DNA fragments and allow DNA to become visible These visible bands of DNA may then be traced photographed
80. or s Manual 14 Magnetic hot plate method Add a stirbar to the undissolved agarose solution Heat the solution to boiling while stirring on a magnetic hot plate Bubbles or foam should be disrupted before rising to the neck of the flask Boil the solution until all of the small transparent agarose particles are dissolved Set aside to cool to 55 60 C before pouring gels c Procedure for Casting Gels This laboratory activity requires that each gel has at least 7 wells Follow the instructions above to prepare the agarose and to determine what volume of 1 agarose will be needed for your class es Pour enough agarose to cover the gel comb teeth or to a depth of 0 5 0 75 cm Do not move or handle the gel tray until the gel has solidified Solidified gels can be stored in sealable bags at room temperature for 1 day or in the refrigerator for up to 1 week before using Have students label their plastic bags The time needed to pour gels by an entire class is approximately 30 minutes If possible pour one or two extra gels for back up This section outlines the tape the tray method for casting gels Other methods are detailed in the Sub Cell GT cell electrophoresis chamber instruction manual i Seal the ends of the gel tray securely with strips of standard laboratory tape not Scotch tape or similar Press the tape firmly to the edges of the gel tray to form a fluid tight seal ii Level the gel tray on a leveling table or workbench using t
81. ote Do not use 0 25x TAE to make agarose gels doing so can lead to a loss of DNA resolution To run gels Place the gel in an electrophoresis chamber and cover it with 0 25x TAE ensure the gel is submerged Run gels at 200 V for no more than 20 min Monitor the movement of gel loading dye to get a relative idea of electrophoresis progress 90 Appendix E Suspect Plasmid Maps Pyull 55 EcoRI 255 BamHI 276 Pstl 298 BamHI 369 Plasmid Maps EcoRV 1448 Scal 3506 EcoRI 1489 Pvull 2022 Psil 2438 Pyull 2541 Hind 2446 Suspect 1 DNA Sample Pvull 55 EcoRI 255 BamHI 276 Pstl 298 Lu 2s m Z LI Q lt Scal 4375 Pyull 1993 Pst 1998 Pstl 2148 Pvyull 3410 Scal 2336 Hind JJ 3315 Pst 3307 Suspect 2 DNA Sample 91 3 XIGNAddV Pvull 55 EcoRI 255 BamHI 276 Pstl 298 EcoRV 403 EcoRI 1118 Scal 5873 Scal 1539 Hindlll 2065 Pyull 4908 HindIII 4813 Pstl 4805 EcoRV 4276 Pvull 4233 Hindill 4092 Crime Scene Suspect 3 DNA Sample Pyull 55 EcoRI 255 BamHI 276 Pstl 298 BamHI 585 Pstl 766 Scal 5765 EcoRV 1763 Pyull 4800 HindIII 4705 Pstl 4697 2913 EcoRV 3166 EcoRV 3904 Pstl 3604 Suspect 4 DNA Sample 92 BamHI 276 Pst 298 Pstl 370 Scal 7987 Pstl 2356 Pstl 2520 Pvull 7022 HindIII 6927 Pstl 6919
82. perience the goals that have been identified above Safety Issues Eating drinking smoking and applying cosmetics are not permitted in the work area Wearing protective eyewear and gloves is strongly recommended Students should wash their hands with soap before and after this exercise If any of the solutions gets into a student s eyes flush with water for 15 minutes Although Fast Blast DNA stain is not toxic latex or vinyl gloves should be worn while handling the stain to keep hands from becoming stained Lab coats or other protective clothing should be worn to avoid staining clothes Storage Temperatures The kit is shipped at room temperature Open immediately upon arrival and store the reagent bag at 20 C within 3 weeks of receipt Kit Inventory Checklist This section lists the equipment and reagents necessary to conduct the Forensic DNA Fingerprinting laboratory We recommend that students be teamed up two to four students per workstation Kit Components Number Kit V 1 Crime Scene CS DNA with buffer lyophilized 60 ug 1 vial m 2 Suspect 1 S1 DNA with buffer lyophilized 60 ug 1 vial m 3 Suspect 2 S2 DNA with buffer lyophilized 60 ug 1 vial m 4 Suspect 3 S3 DNA with buffer lyophilized 60 ug 1 vial a 5 Suspect 4 S4 DNA with buffer lyophilized 60 ug 1 vial m 6 Suspect 5 S5 DNA with buffer lyophilized 60 ug 1 vial a 7 EcoRI Pst restriction enzyme mix lyophilized 3 000 units 1 vial m 8
83. plicity Sample 1 CAGTGATCTCGAATTCGCTAGTAACGTT Sample 2 TCATGAATTCCTGGAATCAGCAAATGCA If both samples are treated with a restriction enzyme recognition sequence GAATTC then indicate the number of fragments and the size of each fragment from each sample of DNA Sample 1 Sample 2 of fragments __ 2 of fragments _ 2 List fragment size in ascending order largest gt smallest Sample 1 Sample 2 17 bp fragment 23 bp fragment 11 bp fragment 5 bp fragment 71 APPENDIX C XIGNAddV Lesson 1 Restriction Digestion of DNA Samples Observation Questions 1 Describe the samples of DNA physical properties The DNA samples are clear colorless liquid samples 2 Is there any observable difference between the samples of DNA No All samples appear similar 3 Describe the appearance of the restriction endonuclease mix The restriction enzymes appear to be clear colorless liquids 72 Lesson 1 Restriction Digestion of DNA Samples Review Questions 1 Before you incubated your samples describe any visible signs of change in the contents of the tubes containing the DNA combined with the restriction enzymes DNA EcoRI Psil enzyme mix APPENDIX C No visible change apparent in the tubes 2 Can you see any evidence to indicate that your samples of DNA were fragmented or altered in any way by the addition of EcoRI Psi Explain No No visible change apparent in the tubes 3 Inthe a
84. r conclusion The DNA samples in lanes 2 and 4 CS and S2 are from the same individual because they have identical restrictions sites that yield identical fragments 75 APPENDIX C Lambda Hindlll size marker Band Distance Actual Distance Approx Distance Approx Distance Approx Distance Approx Distance Approx Distance Approx mm size bp mm size bp mm size bp size bp mm size bp mm size bp size bp mm mm 21 0 21 0 25 0 24 0 28 5 29 5 Ea E a KE M KG an Bi Ee This fragment may appear faint if the markers were not heated to 65 C Lamba Hindlll digestion also generates bands of 564 and 125 bp that are usually too faint to see on a gel The measured migration distance for these bands varies depending upon the thickness of the bands The 2 817 bp bands in plasmids S4 and S5 are especially intense because they are actually two individual bands 2 817 bp and 2 838 bp that are too close to be visibly separated S4 and S5 DNA lanes may also contain a very faint band of 468 bp 76 Size base pairs DNA Standard Band Migration APPENDIX C 10 000 100 0 5 10 15 20 Aa 30 Distance mm To estimate the size of any unknown crime scene or suspect fragment you first need to determine the distances the specific fragment travelled Locate the distance on the x axis of your standard graph For example suspect 5 band 2 migrated 24 mm A From the
85. r digested samples from the refrigerator Using a new tip for each sample add 5 ul of sample loading dye LD to each tube DNA Samples Loading dye Crime Scene CS 5 ul Suspect 1 S1 5 ul Suspect 2 S2 5 ul Suspect 3 S3 5 ul Suspect 4 S4 5 ul Suspect 5 S5 5 ul Loading Dye UTY H F U a cs S1 S2 s3 S4 S5 Flick Tap Tightly cap each tube Mix the components by gently flicking the tubes with your finger If a centrifuge is available pulse spin the tubes to bring the contents to the bottom of the tube Otherwise gently tap the tubes on the table top m Wn e O Z N 2 Cc s m gt Z Cc gt 2 3 Place the casting tray with the solidified gel in it into the platform in the gel box The wells should be at the cathode end of the box where the black lead is connected Very carefully remove the comb from the gel by pulling it straight up 4 Pour 275 ml of electrophoresis buffer into the electrophoresis chamber Pour buffer in the gel box until it just covers the wells of the gel by 1 2 mm 5 Obtain the tube of Hindlll lambda digest DNA marker The loading dye should already have been added by your instructor 32 Student Manual 6 Using a separate pipet tip for each sample load your digested DNA samples into the gel Gels are read from left to right The first sample is loaded in the well at the left hand corner of the gel Lane 1 Lane 2 Lane 3 Lane 4 Lane
86. r to have been cut into the same number and size of fragments 9 Based on your analysis of the example gel drawing on page 35 what is your conclusion about the DNA samples in the drawing Do any of the samples seem to be from the same source If so which ones Describe the evidence that supports your conclusion TWANVIN LNAGNLS v O dp T gt W gt O a lt 40 Student Manual Post Lab Analysis of Results If the overnight staining protocol was used to stain gels record your results and dry gels as described in the gel staining procedures in Lesson 2 page 38 Attach the plastic sheet tracing of the banding patterns from the DNA electrophoresis below Tracing of electrophoresis gel Attach the dried gel showing the banding patterns from the DNA electrophoresis below Dried electrophoresis gel Student Manual ae 52 Ze T0 s lt m be WW aD FO NA TWANVIN LNAGNLS U O a gt W gt O a lt Quantitative Analysis of DNA Fragment Sizes If you were on trial or were trying to identify an endangered species would you want to rely on a technician s eyeball estimate of a match or would you want some more accurate measurement In order to make the most accurate comparison between the crime scene DNA and the suspect DNA other than just a visual match a quantitative measurement of the fragment sizes needs to be completed This is described below 1
87. refore in analyzing how incriminating the DNA evidence is one needs to ask the question Statistically how many people in a population have the same pattern as that taken from a crime scene 1 in 1 000 000 1 in 10 000 Or 1 in 10 Instructor s Manual l lt Z lt o O k O o H 2 Qa ce O oc O xX O lt m u gt O A Q D O Cc z g TWANVIN S HOLONYLSNI Plasmid Mapping Extension The information contained in this kit can be used to perform an optional plasmid mapping activity extension Plasmid mapping is a technique that allows molecular biologists to quickly evaluate the success of cloning experiments and to easily identify plasmids and associated traits in different organisms The crime scene and suspect DNA samples in this kit do not contain human DNA but are constructed using plasmid DNA isolated from bacteria Plasmids are circular non chromosomal pieces of DNA that can replicate in and are commonly found in bacteria and simple eukaryotic organisms such as yeast They typically carry accessory genes separate from the the organism s genomic DNA In nature bacteria evolved plasmids containing genes that enabled them to grow in the presence of antibiotics produced by other micro organisms in the environment This antibiotic resistance gave the bacteria harboring these plasmids a selective advantage over their competitors Bacteria were able to pass the beneficial plasmi
88. resis buffer and swirl to suspend the agarose powder in the buffer If using an Erlenmeyer flask invert a 25 ml flask into the open end of the 500 ml Erlenmeyer flask containing the agarose The small flask acts as a reflux chamber thus allowing long or vigorous boiling without much evaporation The agarose can be melted for gel casting by boiling until agarose has melted completely on a magnetic hot plate hot water bath or in a microwave oven Heated agarose can quickly boil over so watch the process carefully Caution Always wear protective gloves goggles and lab coat while preparing and casting agarose gels Boiling molten agarose or the flasks containing hot agarose can cause severe burns if allowed to contact skin Microwave oven method This technique is the fastest and safest way to dissolve agarose Place the gel solution in an appropriate bottle or flask into the microwave LOOSEN THE CAP IF YOU ARE USING A BOTTLE Use a medium setting and set to 3 minutes Stop the microwave oven every 30 seconds and swirl the flask to suspend any undissolved agarose Boil and swirl the solution until all of the small transparent agarose particles are dissolved Set aside and cool to 55 60 C before pouring Convenient precast agarose gels catalog 161 3057EDU are available from Bio Rad These are 2 x 8 well 1 TAE gels and fit into Bio Rad s Mini Sub Cell GT cell or any horizontal gel electrophoresis system that fits 7 x 10 cm gels Instruct
89. rring a child from its military parents who were kidnappers but who had reared the child for years would be agonizing In practice the transferred children became integrated into their biological families with minimal trauma Identifying organisms that cause disease Eva Harris a UCSF scientist has helped scientists in Nicaragua and Ecuador to learn to use DNA technology to detect tuberculosis and identify the dengue virus and various strains of Leishmania Other available tests cause waits of many weeks while disease organisms are cultured and sent to foreign labs to be identified Marcia Barinaga A Personal Technology Transfer Effort in DNA Diagnostics Science vol 266 1317 1318 Nov 25 1994 Identifying birth parents paternity testing Girls in Florida were discovered to have been switched at birth when one girl died of a hereditary disease The disease was not in her family but was known to be in the family of another girl born in the same hospital and about the same time she was born Proving paternity A woman raped by her employer on Jan 7 1943 her 18th birthday became pregnant The child knew who her father was but as long as he lived he refused to admit being her father After the man died DNA testing proved that she was his daughter and she was granted a half of his estate A Child of Rape Wins Award from Estate of Her Father New York Times July 10 1994 61 APPENDIX A Y XIGNAddV 10
90. s 13 Quick Guide Graphic Laboratory Protocol ccccccsescscseeeeees 20 Student Manual Pre Lab Activity Introduction to DNA Fingerprinting ee 23 Lesson 1 Restriction Digestion of DNA Samples 65 25 Lesson 2 Agarose Gel Electrophoresis of DNA Samples 31 Post Lab Activity Analysis and Interpretation of Results 0 40 Extension Activity 1 Plasmid Mapping ccececseeeeeeeeeneeeeeeesneeeeeeenaes 47 Extension Activity 2 Constructing a Plasmid ccceceeeeeeeeeeeeeeeeeees 55 Appendices Appendix A Alternative DNA Fingerprinting Scenarios 60 Appendix B Prelab Activities cccceeseseceeeeeseeeeeetesseeneeeeeeenes 63 A Review of Restriction Enzymes 0000 63 A Review of Electrophoresis 68 Appendix C Instructor s Answer Guide cccceeeeeereeeeteeeees 70 Appendix D Fast Gel Protocol cccceceseeeeeeeeeeeneeeeeeeeeseeeeeens 90 Appendix E Plasmid Maps nenarocne aae a 91 Appendix F REPEPENCES a e ea a E A 95 Overview for the Instructor Intended Audience This investigation is intended for use by any high school or college student independent of the degree of prior familiarity with the chemistry of nucleic acids Student Objectives That all students who participate in this investigation 1 Become challenged by the task and intrigued by the methodology of the investigation 2 Develop an understanding of some of the basic
91. s do belong to the czar and his family Identification of the remains of the Romanov family by DNA analysis Nature Genetics vol 6 130 1994 60 Determining relatedness of humans DNA typing has shown that the 5 000 year old Iceman found in a melting glacier is most closely related to modern Europeans Iceman Gets Real Science vol 264 1669 June 17 1994 The DNA typing evidence also removes all the suspicions that the body was a fraud that it had been placed on the ice says Svante Paabo of the University of Munich Science vol 264 1775 June 17 1994 Studying relatedness among ancient peoples DNA found at archeological sites in western Montana is being used to help determine how many related groups of people families lived at a particular site Morell Virginia Pulling Hair from the Ground Science vol 265 741 745 August 1994 DNA testing of families DNA testing of families has been used in Argentina and El Salvador to identify the children of at least 9 000 citizens of these countries who disappeared between 1975 and 1983 abducted by special units of the ruling military and police Many of the children born to the disappeared adults were kidnapped and adopted by military parents who claimed to be their biological parents After genetic testing of the extended family revealed the true identity of a child the child was placed in the home of its biological relatives It was feared that transfe
92. s that this is a simulation In actual DNA fingerprinting technicians analyze much larger segments of DNA and many more bands and lanes are produced Reliability of DNA Evidence Two major factors affecting the reliability of DNA fingerprinting technology in forensics are population genetics and genetic statistics In humans there are thousands of RFLP loci or DNA segments that can be selected and used for fingerprinting analysis Depending on demographic factors such as ethnicity or geographic isolation some segments will show more variation than others In general one can assume that any two humans are 99 9 identical DNA sequence Thus they will differ by only 1 bp in 1 000 It is necessary to examine areas that differ to create a useful DNA fingerprint Some populations show much less variation in particular DNA segments than others The degree of variation will affect the statistical odds of more than one individual having the same sequence If 90 of a given population has the same frequency in its DNA fingerprinting pattern for a certain DNA segment then very little information will be attained But if the frequency of a DNA pattern turning up in a population for a particular segment is extremely low then this segment can serve as a powerful tool to discriminate between individuals in that population Different populations show different patterns in their genotypes due to the contributions made to their individual gene pools over time The
93. sample and sample digested with enzyme 2 might not run at exactly the same distance on an agarose gel There is a small difference in migration if a fragment of the same size is uncut circular cut linear or uncut and twisted supercoiled Also fragments that are very similar in size may migrate together in an agarose gel and it may not be possible to distinguish between them In addition fragments that are very small may not be detected by the DNA stain or may run off the end of the gel Reading a Plasmid Map A plasmid map includes information on the size of the plasmid the genes present the origin of replication site and restriction sites for restriction enzymes All five of the plasmids used in the DNA fingerprinting activity were constructed from the same pTZ18U plasmid parent but had different foreign fragments of DNA inserted into them In the DNA fingerprinting exercise only two restriction enzymes were used but other enzymes could also have been used to cut these plasmids The restriction sites are marked on the map with a number that indicates the location of the site Since the plasmid is circular there is an arbitrary zero point All of the restriction sites are indicated with a number between zero and the total base pairs in the plasmid Fragment sizes can then be calculated by simple subtraction and in some cases addition between points on the plasmid Plasmids Used In This Lesson Plasmid maps show the positions numbere
94. scientific principles involved in DNA fingerprinting and analysis of plasmid mapping 3 Weigh evidence and be able to analyze and interpret the data that are generated in this investigation with clarity and confidence 4 Have aclear understanding of the thought processes involved in scientific work 5 Develop the curiosity and confidence to further explore questions and issues involving scientific investigations 6 Use critical thinking to solve problems Teaching Strategies This curriculum is designed to simulate human forensic testing but can also be used to simulate a wide range of applications for genetic analysis The actual scenario employed is up to the discretion of the instructor Refer to alternative scenarios in Appendix A The analysis sections of this investigation are intended to guide students through the process of discovering and understanding concepts that are of significance to the procedures and the analysis of the data at each step along the way It is hoped that this approach as compared to the teacher giving the students all of the background information will make the entire investigation more comprehensible to a greater number of students So long as the teacher has the opportunity to check on the progress and level of understanding of each group some degree of self pacing is possible if so desired We have found that this approach allows a larger number of the diverse population of students we work with to ex
95. ssary You may choose to transfer the rehydrated DNA buffer samples to color coded labeled 1 5 ml microtubes to make pipetting easier for your students The rehydrated DNA samples are now at a concentration of 0 3 yg pl in 100 mM Tris 200 mM NaCl 20 mM MgCl 2 mM DTT pH 8 0 Once the DNA in buffer is added to the enzyme the final concentration of buffer will be 50 mM Tris 100 mM NaCl 10 mM MgCl 1 mM DTT pH 8 0 which is the ideal condition for EcoRI and Pstl enzymes to function Rehydrate lyophilized EcoRI Psi enzyme mix To rehydrate EcoRI Psil enzyme mix add 750 ul sterile water and swirl to resuspend the enzymes Allow enzymes to rehydrate on ice for 5 minutes It is critical that the enzyme mix is kept on ice but not frozen once it has been rehydrated The rehydrated enzymes should be used within 12 hours Aliquot enzyme mix Transfer 80 ul of the rehydrated enzyme mix into each of eight clear 1 5 ml microtubes labeled ENZ Instructor s Manual 13 ape 39 zc F o ceo Oo OO gt 22 ra Ks oA Za TWANVIN S HOLONYLSNI gt S Z 6 m v D a gt gt Z 4 Prepare agarose gels The recommended agarose concentration for gels in this classroom application is 1 agarose This concentration of agarose provides good resolution and minimizes run time required for electrophoretic separation of DNA fragments The recommended thickness for the gel is 0 75 1 0 cm for easy sample loading and gel h
96. stinguish different suspect plasmids and track their spread through the environment DNA from the cultures of a number of stricken patients has been isolated Have your students identify the new killer bug before the pathogen gets out into the general population and starts a true epidemic We strive to continually improve our Biotechnology Explorer kits and curricula Please share your stories comments and suggestions You can download this complete instruction manual on the Internet Visit us on the Web at explorer bio rad com or call us in the US at 1 800 4BIORAD 1 800 424 6723 This curriculum was developed in collaboration with Len Poli and Russ Janigian of the S F Base Biotechnology Program in San Francisco California and Peggy Skinner of the Bush School in Seattle Washington We d like to thank them for their invaluable guidance and contributions to this curriculum Ron Mardigian Biotechnology Explorer Program Bio Rad Life Science Group 2000 Alfred Nobel Drive Hercules California 94547 Create context Reinforce learning Stay current New scientific discoveries and technologies create more content for you to teach but not more time Biotechnology Explorer kits help you teach more effectively by integrating multiple core content subjects into a single lab Connect concepts with techniques and put them into context with real world scenarios Use of restriction enzymes and electrophoresis to fingerprint DNA Use o
97. t Blast DNA stain 500x 100 ml catalog 166 0420EDU Molecular biology agarose 25 g catalog 161 3100EDU DNA fingerprinting kit refill package catalog 166 0027EDU contains crime scene and suspect DNA samples EcoRI Psil restriction enzyme mix sample loading buffer Fast Blast DNA stain DNA markers sterile water EcoRI Pstl restriction enzyme mix catalog 166 0047EDU Small DNA Electrophoresis Reagent Pack catalog 166 0450EDU to pour run amp stain 48 1 or 16 3 7x10 cm agarose gels Medium DNA Electrophoresis Reagent Pack catalog 166 0455EDU to pour run amp stain 270 1 or 90 3 7x10 cm agarose gels Large DNA Electrophoresis Reagent Pack catalog 166 0460EDU to pour run amp stain 1080 1 or 360 3 7x10 cm agarose gels Ow gt O A Q J O Cc zZ g TWANVIN S HOL NYLSNI Instructors Manual Background Introduction Technicians working in forensic labs are often asked to do DNA profiling or fingerprinting to analyze evidence in law enforcement cases and other applications Restriction Fragment Length Polymorphism RFLP has been the workhorse of forensic DNA profiling for many years First described by English geneticist Alec Jeffries in 1985 RFLP analysis provides a unique banding pattern based on the restriction sites present in an individuals DNA sequence Currently DNA profiling involves polymerase chain reaction PCR amplification which allows the analysis of minute quantities of DNA in a muc
98. t differences in their linear base pair sequence Now that you have a fairly clear understanding of these three items you are ready to proceed to the first phase of the DNA fingerprinting procedure performing a restriction digest of your DNA samples Your Workstation Checklist Make sure the materials listed below are present at your lab station prior to beginning the lab a lt Z lt Z Lu m H d9 z O i e W l Material Needed for Each Workstation Quantity V Agarose gel electrophoresis system electrophoresis 1 m chamber casting tray 8 well comb EcoRI Psti enzyme mix 1 tube 80 yl O Pipet tips 2 200 pl 15 tips Q Micropipet 2 20 ul 1 m Colored micro test tubes green blue orange violet red yellow 1 m Permanent marker 1 m Waste container 1 Q Foam micro test tube holder 1 m Laboratory tape not 3M Scotch brand or similar tape 1 Q Instructor s Workstation Crime scene DNA with buffer rehydrated 1 vial m Suspect 1 DNA with buffer rehydrated 1 vial m Suspect 2 DNA with buffer rehydrated 1 vial m Suspect 3 DNA with buffer rehydrated 1 vial O Suspect 4 DNA with buffer rehydrated 1 vial m Suspect 5 DNA with buffer rehydrated 1 vial O Molten 1 agarose in 1x TAE See Advance Prep 40 50 ml per gel m 37 C water bath or incubator optional 1 per class Q Microcentrifuge 1 per class m or mini centrifuge 4 per class O Student Manual 27 Observations
99. t plasmid You will use EcoRI for the construction and need to refer to the lambda bacteriophage genome map that includes the EcoRI sites You must make a plasmid that is at least 5 000 base pairs but not more than 10 000 base pairs in size Remember that the parent plasmid is 2860 bp in size Where is the EcoRI site on the parent pTZ18U plasmid 6 Choose a segment of lambda bacteriophage genome that could be cut out by the EcoRI enzyme Which segment will you use Student Manual 58 7 Draw your new plasmid with the insert of your choice Be sure to include the restriction sites for Pstl and EcoRI in your drawing How big is your new plasmid Give the positions of the restriction sites in your new plasmid a number indicating the location Remember that the first EcoRI site will still be position 255 as it is in the parent pTZ18U plasmid map N gt E How many restriction sites are there now for Psi in your new plasmid Predict what i fragments you would generate if you were to digest your plasmid with 2 z l O i EcoRI alone Zon WZ Ow ls Ee x V W ii Pstl alone iii EcoRI and Psi together a double digest Draw an agarose gel for each of these digests and label the fragment sizes The lambda phage fragment can be inserted into the host plasmid in either orientation forwards or backwards How could you use plasmid mapping to determine in which orientation your fragment was inserted Use a diagram in your
100. tic Fingerprinting Pauline Lowrie and Susan Wells New Scientist 16 November 1991 Is DNA Fingerprinting ready for the courts William C Thompson and Simon Ford New Scientist March 31 1990 When Science Takes the Witness Stand Peter Neufeld and Nevelle Coleman Scientific American Vol 262 5 May 1990 Using Restriction Mapping to Teach Basic Skills in the Molecular Biology Lab Lauren Walsh Elizabeth Shakir and Elizabeth A De Stasio Biochemistry and Molecular Biology Education Vol 35 No 3 pp 199 205 2007 APPENDIX F 95 Life Science Group Bio Rad Laboratories Inc Web site www bio rad com USA 800 4BIORAD Australia 61 02 9914 2800 Austria 01 877 89 01 Belgium 09 385 55 11 Brazil 55 21 3237 9400 Canada 905 712 2771 China 86 21 6426 0808 Czech Republic 420 241 430 532 Denmark 44 52 10 00 Finland 09 804 22 00 France 01 47 95 69 65 Germany 089 318 840 Greece 30 210 777 4396 Hong Kong 852 2789 3300 Hungary 36 1 455 8800 India 91 124 4029300 Israel 03 963 6050 Italy 39 02 216091 Japan 03 5811 6270 Korea 82 2 3473 4460 Mexico 52 555 488 7670 The Netherlands 0318 540666 New Zealand 0508 805 500 Norway 23 38 41 30 Poland 48 22 331 99 99 Portugal 351 21 472 7700 Russia 7 495 721 14 04 Singapore 65 6415 3188 South Africa 27 861 246 723 Spain 34 91 5905200 Sweden 08 555 12700 Switzerland 061 717 95 55 Taiwan 886 2 2578 7189 United Kingdom 020 8328 2000 Sig 1106 4006096 Rev G
101. tock tubes and transfer to the corresponding colored micro test tubes Make sure the sample is transferred to the bottom of the tubes 4 Pipet 10 ul of enzyme mix ENZ into the very bottom of each tube Use a fresh tip to transfer the ENZ sample to each tube Pipet up and down carefully to mix well 5 Tightly cap the tubes and mix the components by gently flicking the tubes with your finger If a microcentrifuge is available pulse spin in the centrifuge to collect all the liquid in the bottom of the tube Otherwise gently tap the tube on the table top 6 Place the tubes in the foam micro tube holder and incubate for 45 min at 37 C or overnight at room temperature in a large volume of water heated to 37 C 7 If required follow the instructors directions to pour a 1 agarose gel 8 After the incubation period remove the tubes from the water bath and place in the refrigerator until the next laboratory period If there is sufficient time to continue proceed directly to step 2 of Lesson 2 Student Manual LSO v ENZ eS 20 i jil vy Water bath Enzyme Mix DNA Samples eS 7 Flick Tap Lesson 2 Agarose Gel Electrophoresis 1 Remove the digested DNA samples from the refrigerator if applicable If a centrifuge is available pulse spin the tubes in the centrifuge to bring all of the liquid into the bottom of the tube or g
102. uanine and cytosine Are the bases paired in an identical manner in all three samples Describe the pattern of the base pair bonding The adenine is always bonded with thymine and the cytosine is always bonded with the guanine In your attempt to analyze DNA samples from three different individuals what conclusions can you make about the similarities and differences of the DNA samples The sugar phosphate arrangement is the same for all samples and so are the kind of bases what is different is the arrangement of bases among the three samples What will you need to compare between these DNA samples to determine if they are identical or non identical The sequence of base pairs in each individual sample 70 Lesson 1 Restriction Digests of DNA Samples 1 How many pieces of DNA would result from this cut 2 2 Write the base sequence of the DNA fragments on both the left and right side of the cut ATG AATTCTCAATTACCT TACTTAA GAGTTAATGGA 3 What differences are there in the two pieces Each fragment is a different size 4 DNA fragment size can be expressed as the number of base pairs in the fragment Indicate the size of the fragments mention any discrepancy you may detect One fragment is short and one is long also some bases are unpaired a Thesmallerfragmentis_ 3 base pairs bp b What is the length of the longer fragment __11 5 Consider the two samples of DNA shown below single strands are shown for sim
103. ubes on the lab bench will also help to combine and mix the contents Y g I g U g I cs Si S2 S3 S4 s5 Flick Tap 6 Incubate the samples Place the tubes in the foam micro tube holder and incubate them at 37 C for 45 minutes Alternatively the tubes can be incubated in a large volume of water heated to 37 C and allowed to slowly reach room temperature overnight After the incubation store the DNA digests in the refrigerator until the next lab period or proceed directly to step 2 of Lesson 2 if instructed by your teacher lt Z lt Z Lu m H Z O 7 Y Ww j mn Water bath Note While you are waiting this is a good time to cast your agarose gel unless they have already been prepared for you Check with your teacher for the proper procedure Student Manual 29 Lesson 1 Restriction Digestion of DNA Samples Review Questions 1 Before you incubated your samples describe any visible signs of change in the contents of the tubes containing the DNA after it was combined with the restriction enzymes 2 Can you see any evidence to indicate that your samples of DNA were fragmented or altered in any way by the addition of EcoRI Psi Explain m op wn O a ep Cc g m gt Z Cc gt m 3 Inthe absence of any visible evidence of change is it still possible that the DNA samples were fragmented Explain your reasoning 4 Answer the next day
104. urable record of the experiment Gel Support Film es 32 Zq T o fs Pw CoO gt 22 cea FS nO Zq Note Avoid extended exposure of dried gels to direct light to prevent band fading However DNA bands will reappear if the dried gels are stored in the dark for 2 3 weeks after fading Graphing the Data Many of your students may not be familiar with logarithms and semilog graph paper It is suggested that you prepare a short lesson to demonstrate the proper way to label the coordinates and plot the points You might also choose to discuss the advantage of using semilog vs standard graph paper in this instance A math extension here can also provide an opportunity to explore linear and exponential arithmetic and geometric sequences of numbers We have included semilog graph paper on page 44 of this manual Instructor s Manual 19 AGINS AINO Forensic DNA Fingerprinting Kit Quick Guide Lesson 1 Restriction Digestion 1 Place the tube containing the restric tion enzyme mix labeled ENZ on ice 2 Label one of each colored micro test tubes as follows green tube CS crime scene blue tube S1 suspect 1 orange tube S2 suspect 2 violet tube S3 suspect 3 red tube S4 suspect 4 yellow tube S5 suspect 5 Label the tubes with your name date and lab period Place the tubes in the foam micro test tube holder 3 Using a fresh tip for each sample pipet 10 pl of each DNA sample from the s

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