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Forensic DNA Fingerprinting: Using Restriction Enzymes

Forensic DNA Fingerprinting: Using Restriction Enzymes. Forensic DNA Fingerprinting Kit Instructors. Stan Hitomi Coordinator – Math & Science San Ramon Valley Unified School District Danville, CA Kirk Brown Lead Instructor, Edward Teller Education Center

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Forensic DNA Fingerprinting: Using Restriction Enzymes

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  1. Forensic DNA Fingerprinting: Using Restriction Enzymes

  2. Forensic DNA Fingerprinting KitInstructors Stan Hitomi Coordinator – Math & Science San Ramon Valley Unified School District Danville, CA Kirk Brown Lead Instructor, Edward Teller Education Center Science Chair, Tracy High School and Delta College, Tracy, CA Sherri Andrews, Ph.D. Curriculum and Training Specialist Bio-Rad Laboratories Essy Levy, M.Sc. Curriculum and Training Specialist Bio-Rad Laboratories

  3. WhyTeach DNA Fingerprinting? • Real-world connections • Tangible results • Link to careers and industry • Laboratory extensions • Standards-based

  4. Forensic DNA Fingerprinting Kit Advantages • Standards Based • Aligns with AP Biology Lab 6 • Use of real restriction enzymes and electrophoresis of real DNA fragments • Lab can completed in two 45 minute sessions • Sufficient materials for 8 student workstations

  5. The Forensic DNA Fingerprinting Kit Can HelpYou Teach: • DNA structure • DNA restriction analysis (RFLP) • Agarose gel electrophoresis • Molecular weight determination • Simulation of DNA Fingerprinting • Plasmid mapping

  6. DNA Fingerprinting Real WorldApplications • Crime scene • Human relatedness • Paternity • Animal relatedness • Anthropology studies • Disease-causing organisms • Food identification • Human remains • Monitoring transplants

  7. Workshop Time Line • Restriction digest of DNA samples • Introduction to DNA Fingerprinting and RFLP analysis • Electrophoresis on Agarose gels • Analysis and interpretation of results

  8. DNA FingerprintingProcedureOverview

  9. LaboratoryQuick Guide

  10. DNA Fingerprinting ProceduresDay One

  11. DNA Fingerprinting ProceduresDay Two

  12. DNA Fingerprinting ProceduresDay Three

  13. DNA is Tightly Packaged into Chromosomes Which Reside in the Nucleus

  14. Model of DNADNA is Comprised of Four Base Pairs

  15. Deoxyribonucleic Acid (DNA)

  16. DNASchematic O Phosphate O P O Base O O CH2 Sugar O O O P Phosphate Base O O CH2 Sugar OH

  17. DNA Restriction Enzymes • Evolved by bacteria to protect against viral DNA infection • Endonucleases = cleave within DNA strands • Over 3,000 known enzymes

  18. Enzyme Site Recognition Restriction site Palindrome • Each enzyme digests (cuts) DNA at a specific sequence = restriction site • Enzymes recognize 4- or 6- base pair, palindromic sequences (eg GAATTC) Fragment 2 Fragment 1

  19. 5 vs 3 Prime Overhang Enzyme cuts • Generates 5 prime overhang

  20. Common Restriction Enzymes EcoRI – Eschericha coli – 5 prime overhang Pstl – Providencia stuartii – 3 prime overhang

  21. The DNA DigestionReaction Restriction Buffer provides optimal conditions • NaCI provides the correct ionic strength • Tris-HCI provides the proper pH • Mg2+ is an enzyme co-factor

  22. DNA DigestionTemperature Why incubate at 37°C? • Body temperature is optimal for these and most other enzymes What happens if the temperature is too hot or cool? • Too hot = enzyme may be denatured (killed) • Too cool = enzyme activity lowered, requiring longer digestion time

  23. PstI EcoRI Restriction Fragment Length PolymorphismRFLP GAATTC GTTAAC CTGCAG GAGCTC Allele 1 1 2 3 CGGCAG GCGCTC GAATTC GTTAAC Allele 2 3 Fragment 1+2 Different Base Pairs No restriction site M A-1 A-2 Electrophoresis of restriction fragments M: Marker A-1: Allele 1 Fragments A-2: Allele 2 Fragments +

  24. AgaroseElectrophoresisLoading • Electrical current carries negatively-charged DNA through gel towards positive (red) electrode Buffer Dyes Agarose gel Power Supply

  25. AgaroseElectrophoresisRunning • Agarose gel sieves DNA fragments according to size – Small fragments move farther than large fragments Gel running Power Supply

  26. Analysis of Stained Gel Determine restriction fragment sizes • Create standard curve using DNA marker • Measure distance traveled by restriction fragments • Determine size of DNA fragments Identify the related samples

  27. Molecular Weight Determination Fingerprinting Standard Curve: Semi-log Size (bp) Distance (mm) 23,000 11.0 9,400 13.0 6,500 15.0 4,400 18.0 2,300 23.0 2,000 24.0

  28. DNA Fingerprinting Lab Extensions • Independent studies • Plasmid DNA isolation (mini-preps) • Plasmid mapping using restriction enzymes • Southern blot analysis • Introductory labs to electrophoresis: Kool-Aid/FastBlast pH indicator in buffer

  29. 863bp 863bp 3469bp 2027bp Hind III BamHI 947bp EcoRI 721bp 721bp 7367bp 2027bp 1659bp EcoRI+ HindIII 6504bp Plasmid Mapand Restriction SitesLaboratory Extensions BamHI: EcoRI: HindIII: EcoRI+Hind III: 1 linear fragment; 7367bp 2 fragments; 863bp / 6504bp 3 fragments; 721bp/2027bp/3469bp 5 fragments; 721bp/863bp/947bp/1659bp/2027bp

  30. Bio-Rad’sElectrophoresisEquipment • Electrophoresis Cells • Power Supplies • Precast Agarose Gels PowerPac™ Mini PowerPac™ Basic PowerPac™ HC PowerPac™ Universal Mini-Sub® Cell GT Wide Mini-Sub Cell GT

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