1. Chapter 9 DNA: The Indispensable Forensic Science Tool

2. Introduction 1985-Sir Alex Jeffreys recognized that portions of DNA structure of certain genes are unique to each individual. 1985-Sir Alex Jeffreys recognized that portions of DNA structure of certain genes are unique to each individual. The process of identifying these markers is known as DNA fingerpringting, DNA typing, or DNA profiling The process of identifying these markers is known as DNA fingerpringting, DNA typing, or DNA profiling Forensic Scientists now had a way of linking biological samples like blood, semen, hair, and tissue to a single individual Forensic Scientists now had a way of linking biological samples like blood, semen, hair, and tissue to a single individual US courts have accepted the reliability of DNA evidence US courts have accepted the reliability of DNA evidence

3. DNA = Deoxyribonucleic Acid DNA is a polymer DNA is a polymer Polymers are very large molecules put together by linking units called monomers Polymers are very large molecules put together by linking units called monomers The monomers of DNA are called nucleotides. The monomers of DNA are called nucleotides.

4. Nucleotides DNA nucleotides consist of : DNA nucleotides consist of : A sugar molecule that forms the backbone A sugar molecule that forms the backbone A phosphate group which links the sugars A phosphate group which links the sugars A nitrogen containing base (adenine, cystine, guanine, thymine) A nitrogen containing base (adenine, cystine, guanine, thymine) Nucleotides are linked together to form a double helix Nucleotides are linked together to form a double helix What is DNA? What is DNA?

5. Complementary Base Pairing Adenine always pairs with Thymine Adenine always pairs with Thymine Guanine always pairs with Cytosine Guanine always pairs with Cytosine Bases are joined together by hydrogen bonding. Bases are joined together by hydrogen bonding.

6. How DNA works DNA directs the production of proteins which play a basic role in the structure and function of living organisms DNA directs the production of proteins which play a basic role in the structure and function of living organisms Proteins are built by linking amino acids Proteins are built by linking amino acids The are 20 amino acids that make up proteins The are 20 amino acids that make up proteins The sequence of amino acids determines the shape and function of the protein The sequence of amino acids determines the shape and function of the protein

7. How DNA works Each amino acid is coded by a sequence of 3 bases Each amino acid is coded by a sequence of 3 bases

8. Replication of DNA Replication – synthesis of new DNA from existing DNA Replication – synthesis of new DNA from existing DNA The double helix is unwound and a copy is made. The double helix is unwound and a copy is made. DNA polymerase – DNA polymerase – Assemble new DNA strands in the proper base sequence Assemble new DNA strands in the proper base sequence Correct mismatched base pairs Correct mismatched base pairs

9. Polymerase Chain Reaction (PCR) A technique for replicating a portion of DNA outside of a living cell A technique for replicating a portion of DNA outside of a living cell DNA polymerases are used to make copies of DNA material DNA polymerases are used to make copies of DNA material This is useful to forensic scientists because small samples could be multiplied. This is useful to forensic scientists because small samples could be multiplied.

10. DNA Typing with Tandem Repeats Tandem repeat –sequence of base pairs repeated numerous times. Tandem repeat –sequence of base pairs repeated numerous times. ~30 % of human genome is made up of tandem repeats. ~30 % of human genome is made up of tandem repeats. They act as spacers in between coding regions of the DNA They act as spacers in between coding regions of the DNA Used by forensic scientists to distinguish individuals. Used by forensic scientists to distinguish individuals.

11. DNA Typing with Tandem Repeats Humans have the same type of repeats but a wide variety in the number of repeats. Humans have the same type of repeats but a wide variety in the number of repeats. Restriction fragment length polymorphisms (RFLP’s) – repeat segments cut out of DNA by restriction enzymes. Restriction fragment length polymorphisms (RFLP’s) – repeat segments cut out of DNA by restriction enzymes.

12. DNA Typing with Tandem Repeats Length differences associated with RFLP’s allow forensic scientists to identify individuals. Length differences associated with RFLP’s allow forensic scientists to identify individuals. Electrophoresis is used to separate different sized fragments. Electrophoresis is used to separate different sized fragments. Gel Electrophoresis Gel Electrophoresis Gel Electrophoresis Gel Electrophoresis

13. DNA Typing with Tandem Repeats

14. Polymerase Chain Reaction (PCR) PCR replaced RFLP techniques in the mid- 1990’s PCR replaced RFLP techniques in the mid- 1990’s The Basics: Short DNA sequences are identified. Short DNA sequences are identified. DNA strands are unwound and replicated yielding two copies of the original sample DNA strands are unwound and replicated yielding two copies of the original sample 28-32 cycles are carried out yielding over a billion copies of the DNA strand. 28-32 cycles are carried out yielding over a billion copies of the DNA strand. Polymerase Chain Reaction Polymerase Chain Reaction

15. Polymerase Chain Reaction (PCR) Advantages of PCR over RFLP typing: 1. PCR uses much smaller strands of DNA 2. Smaller strands are more stable and less subject to degradation 3. Smaller strands overcome the sample- size problem associated with crime-scene evidence

16. Short Tandem Repeats (STR’s) STR’s – DNA profiling procedure used currently STR’s – DNA profiling procedure used currently Short Tandem Repeats – regions of DNA molecules containing short segments of 3 to 7 repeating base pairs. Short Tandem Repeats – regions of DNA molecules containing short segments of 3 to 7 repeating base pairs. STR’s are less susceptible to degradation and can be amplified by PCR STR’s are less susceptible to degradation and can be amplified by PCR Multiplexing: A technique that simultaneously detects more than one DNA marker in a single analysis. Multiplexing: A technique that simultaneously detects more than one DNA marker in a single analysis.

17. Short Tandem Repeats (STR’s) In the US, the forensic science community has standardized 13 STR’s for entry into the CODIS database In the US, the forensic science community has standardized 13 STR’s for entry into the CODIS database FBI Core STR Loci FBI Core STR Loci FBI Core STR Loci FBI Core STR Loci Calculating the frequency of occurence of a DNA profile Calculating the frequency of occurence of a DNA profile Calculating the frequency of occurence of a DNA profile Calculating the frequency of occurence of a DNA profile Separation of STR's by capillary electrophoresis Separation of STR's by capillary electrophoresis Separation of STR's by capillary electrophoresis Separation of STR's by capillary electrophoresis Results of electrophoresis on STR's Results of electrophoresis on STR's Results of electrophoresis on STR's Results of electrophoresis on STR's

18. Sex Identification Using STR’s The sex of a DNA contributor can be determined by looking at the amelogenin gene. The gene is 6 bases shorter on the X chromosome than it is on the Y chromosome. The sex of a DNA contributor can be determined by looking at the amelogenin gene. The gene is 6 bases shorter on the X chromosome than it is on the Y chromosome. Y-STR’s – STR’s found on the Y chromosome; useful when there is a mix of DNA from more than one male. Y-STR’s – STR’s found on the Y chromosome; useful when there is a mix of DNA from more than one male.

19. Mitochondrial DNA Mitochondrial DNA (mtDNA) – found in the mitochondria (outside of the cell nucleus) Mitochondrial DNA (mtDNA) – found in the mitochondria (outside of the cell nucleus) mtDNA is inherited solely from the mother mtDNA is inherited solely from the mother Forensic Scientists use mtDNA to identify subjects when nuclear DNA is not available. Forensic Scientists use mtDNA to identify subjects when nuclear DNA is not available. Frequencies of sequences in the FBI database are about 1 % Frequencies of sequences in the FBI database are about 1 % inheritance of mtDNA inheritance of mtDNA inheritance of mtDNA inheritance of mtDNA structure of mtDNA structure of mtDNA structure of mtDNA structure of mtDNA

20. The Combined DNA Index System (CODIS) CODIS – software program and database developed by the FBI CODIS – software program and database developed by the FBI Contains DNA profiles of convicted offenders, unsolved crime-scene evidence, and profiles of missing people. Contains DNA profiles of convicted offenders, unsolved crime-scene evidence, and profiles of missing people.

21. Collection and Preservation of DNA Evidence STR profiling requires only 125 picograms of DNA STR profiling requires only 125 picograms of DNA One human cell contains ~ 7 pg of DNA One human cell contains ~ 7 pg of DNA Only 18 cells are necessary Only 18 cells are necessary As a result, DNA has been successfully analyzed from stamps, envelopes, cups, cigarette butts, chewing gum, skin cells, etc. As a result, DNA has been successfully analyzed from stamps, envelopes, cups, cigarette butts, chewing gum, skin cells, etc.

22. Collection and Preservation of DNA Evidence Biological evidence should be documented by notes, sketches, and photographs first Biological evidence should be documented by notes, sketches, and photographs first The shape and position of bloodstains should be investigated prior to collection. The shape and position of bloodstains should be investigated prior to collection. Latex gloves will protect investigators from infection AND avoid contaminating the evidence. Latex gloves will protect investigators from infection AND avoid contaminating the evidence. Items like clothing should be collected from suspects and victims even if blood isn’t immediately visible. Items like clothing should be collected from suspects and victims even if blood isn’t immediately visible.

23. Collection and Preservation of DNA Evidence Packaging of Evidence: Biological evidence should not be packaged in an airtight container; paper bags, envelopes, or cardboard boxes can be used. Samples should be refrigerated and kept out of direct sunlight Biological evidence should not be packaged in an airtight container; paper bags, envelopes, or cardboard boxes can be used. Samples should be refrigerated and kept out of direct sunlight Blood stains can be removed from a surface using a cotton swab soaked in distilled water. Blood stains can be removed from a surface using a cotton swab soaked in distilled water. Swabs must be dried prior to packaging Swabs must be dried prior to packaging

24. Collection and Preservation of DNA Evidence Obtaining DNA Reference Samples: Reference samples can be obtained by collecting blood or a buccal swab from an individual Reference samples can be obtained by collecting blood or a buccal swab from an individual If the individual is not available: If the individual is not available: Tootbrush Tootbrush Combs and hairbrushes Combs and hairbrushes Razor Razor Dirty laundry Dirty laundry Cigarette butts Cigarette butts

25. Collection and Preservation of DNA Evidence To minimize contamination: Change gloves before handling each new piece of evidence Change gloves before handling each new piece of evidence Collect a substrate control. Collect a substrate control. Use forceps to pick up small items Use forceps to pick up small items Package items is individual well-ventilated containers. Package items is individual well-ventilated containers. Luminol does not destroy DNA Luminol does not destroy DNA