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Published byPhebe Cannon Modified over 9 years ago
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Forensic Analysis of DNA Chapter 9
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DNA Genetic Material Double stranded; two strands of nucleotides http://www.youtube.com/watch?v=ZGHkHMoyC5I http://www.youtube.com/watch?v=ZGHkHMoyC5I Nucleotides have phosphate group, deoxyribose sugar, and nitrogenous base (adenine, thymine, guanine, and cytosine) DNA is copied into new DNA through DNA replication in nucleus http://www.youtube.com/watch?v=teV62zrm2P0 http://www.youtube.com/watch?v=teV62zrm2P0 DNA is transcribed into mRNA in nucleus; mRNA is converted to proteins through translation at the ribosome
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DNA Replication
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Transcription—DNA to mRNA
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Restriction Enzymes Cut DNA has specific recognition sequence Extracted from bacteria Gives fragments of different sizes http://www.youtube.com/watch?v=lPdQwdG gyfQ http://www.youtube.com/watch?v=lPdQwdG gyfQ
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Restriction Enzymes
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Polymerase Chain Reaction Makes many copies of small collected DNA samples Done prior to other testing Uses DNA polymerase, 2 kinds of primers, free nucleotides, and thermal cycler Uses heating to denature and cooling for annealing Can get 2 n DNA double helices where n is the number of heating and cooling cycles http://www.youtube.com/watch?v=v4L7rvmBXb Y http://www.youtube.com/watch?v=v4L7rvmBXb Y
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PCR
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Repetitive DNA When during DNA typing, want to use non- coding repetitive DNA; not coding DNA Much more variation in non-coding DNA Tandem repeats; non-coding repetitive DNA VNTR—variable number tandem repeats; often used for DNA typing STR—short tandem repeats; used most often for DNA typing RFLP—restriction fragment length polymorphism; cut with restriction enzymes to make many fragments
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VNTR
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STR
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RFLP
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Electrophoresis Load negative DNA at black side of chamber into gel (agarose or polyacrylamide) DNA moves to positive electrode Small fragments move farther through the gel Buffer is used as electrolyte to help send current through gel http://www.youtube.com/watch?v=0x2Lh5Rq 8e0&feature=related http://www.youtube.com/watch?v=0x2Lh5Rq 8e0&feature=related
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Electrophoresis
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DNA Typing--Identification http://www.youtube.com/watch?v=RCI9Yhs tHK4&feature=fvw
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Crime Scene DNA Analysis
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DNA Typing—Paternity Testing
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Paternity Testing
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Hybridization DNA from electrophoretic gel is transferred to nylon membrane or paper filter DNA can be heated to be denatured Radioactive or fluorescent probe are used to find specific DNA section
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Hybridization
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DNA Typing Amplify with PCR Use restriction enzymes to make RFLPs of STR or VNTR sequence of genome Separate fragments with electrophoresis Match bands with known samples to determine identity Can be used for crime scene matching, paternity testing, and identifying corpses or body parts
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CODIS STR data for first 13 STRs are put into CODIS If use at least 6 STRs, matching process is very precise; 1 in 2,000,000 probability; Using all 13 makes the probability of an incorrect match being 1 in 575-900 trillion
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CODIS STRs
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Capillary Electrophoresis Use glass capillary tube with gel wrapping and buffer reservoir STRs move through column and as pass through column peak appears on attached computer instrument Peak diagram is called an electropherogram
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STR used for gender identification Uses amelogenin gene whose length is different in X and Y chromosome STR electrophoresis shows two separate bands for presence of X and Y chromosome in males Shows one band for 2 X chromosomes in females
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Gender ID with STR
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mtDNA Found outside nucleus is mitochondria Easier to get and can be taken from any relative of the same maternal lineage Same in all relatives from same maternal line; so not as specific of a match Can be gotten when burning, age, or environmental degradation has damaged genomic DNA
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Mitochondrial DNA
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DNA sources for collection Any cells from skin, in blood, cheek cells from saliva, epithelial cells in hair follicles Sweat, semen, ear war, mucus can also be used to extract cells for DNA typing
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Collection of Biological Evidence Photograph, sketch, describe, and collect Collect from body fluids, tissues, trash, laundry, placed often touched (handles, light switches; places licked (envelopes, lipstick, cigarettes, partially eaten food for drink); places where body fluids might be (clothing, tissues, sheets, pillows, condoms)
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DNA Evidence Package each DNA stained item separately in paper bag or well-ventilated container; closed containers can lead to moisture and growth of DNA digesting bacteria Obtain reference DNA—buccal cells or blood Avoid contamination—wear gloves; never cross-contaminate DNA from one piece of evidence with another; use different instruments for every piece of evidence
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