Title: Forensic%20DNA%20Fingerprinting:
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2Forensic DNA Fingerprinting Using Restriction
Enzymes
3Forensic DNA Fingerprinting KitInstructors
- Stan Hitomi
- Coordinator Math Science
- Principal Alamo School
- 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
- Bio-Rad Curriculum and Training Specialists
- Sherri Andrews, Ph.D.
- sherri_andrews_at_bio-rad.com
- Leigh Brown, M.A.
- leigh_brown_at_bio-rad.com
4Why Teach DNA Fingerprinting?
- Real-world connections
- Tangible results
- Link to careers and industry
- Laboratory extensions
- Standards-based
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6Forensic 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
7The Forensic DNA Fingerprinting Kit Can Help You
Teach
- DNA structure
- DNA restriction analysis (RFLP)
- Agarose gel electrophoresis
- Molecular weight determination
- Simulation of DNA Fingerprinting
- Plasmid mapping
8DNA Fingerprinting Real WorldApplications
- Crime scene
- Human relatedness
- Paternity
- Animal relatedness
- Anthropology studies
- Disease-causing organisms
- Food identification
- Human remains
- Monitoring transplants
9Workshop Time Line
- Restriction digest of DNA samples
- Introduction to DNA Fingerprinting and RFLP
analysis - Electrophoresis on Agarose gels
- Analysis and interpretation of results
10DNA FingerprintingProcedureOverview
11LaboratoryQuick Guide
12DNA Fingerprinting ProceduresDay One
13DNA Fingerprinting ProceduresDay Two
14DNA Fingerprinting ProceduresDay Three
15DNA is Tightly Packaged into Chromosomes Which
Reside in the Nucleus
16Model of DNADNA is Comprised of Four Base
Pairs
17Deoxyribonucleic Acid (DNA)
18DNA Schematic
O
Phosphate
P
O
O
Base
O
O
CH2
Sugar
O
P
O
O
Phosphate
Base
O
O
CH2
Sugar
OH
19DNA Restriction Enzymes
Evolved by bacteria to protect against viral
DNA infection Endonucleases cleave within
DNA strands Over 3,000 known enzymes
20Enzyme 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
215 vs 3 Prime Overhang
Enzyme cuts
Generates 5 prime overhang
22Common Restriction Enzymes
EcoRI Eschericha coli 5 prime overhang
Pstl Providencia stuartii 3 prime overhang
23The 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
24DNA DigestionTemperature
- Why incubate at 37C?
- 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
25Restriction Fragment Length PolymorphismRFLP
PstI
EcoRI
GAATTC CTTAAG
CTGCAG GACGTC
Allele 1
1
2
3
GAATTC CTTAAG
CGGCAG GCCGTC
Allele 2
3
Fragment 12
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
26AgaroseElectrophoresisLoading
- Electrical current carries negatively-charged
DNA through gel towards positive (red) electrode
Buffer
Dyes
Agarose gel
Power Supply
27AgaroseElectrophoresisRunning
- Agarose gel sieves DNA fragments according to
size - Small fragments move farther than large
fragments
Gel running
Power Supply
28Chemistry in action.OrAsk your friendly
chemistabout electro-phoresis
andelectrolysis.
29Chemistry of electrophoresis and
electrolysisElectric fieldsand electric
currents
30SDS-PAGE, DNA electrophoresis and the need for a
gel matrix (sieving medium)Without a viscous
medium, all molecules move at the same rate in
electric fieldGel structure retards larger
solute particlesDNA molecules, SDS- proteins
have equal charge/massElectrophoresis occurs
between the electrodes (field-driven).
31Electrolysis always occurs during
electro-phoresis.Cathode produces H2 at twice
the rate that anode produces O2Current is
carried by solute ions. Electrons arent soluble
in H2O.Example TAE buffer tris
suppliescations (), acetatesupplies anions
(-).Electrolysis occursat the electrodes.
32Analysis 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
33Analysis using Verniers Logger Pro
softwareAdaptable to many forms of Gel
Analysis Take or Import Gel Image Set
Origin Set Scale Set Standard Ladder Add
LanesLeaves more time for students to Explore
34Standard Curve and AnalysisEasy to View Results
include Gel Image Standard Curve
Data Table One convenient page with all the
Results
35Molecular 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
36DNA 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
37Plasmid Mapand Restriction SitesLaboratory
Extensions
BamHI EcoRI HindIII EcoRIHind III
1 linear fragment 7367bp
2 fragments 863bp / 6504bp
3 fragments 721bp/2027bp/3469bp
5 fragments
721bp/863bp/947bp/1659bp/2027bp
38Bio-RadsElectrophoresisEquipment
PowerPac Mini
PowerPac Basic
- Electrophoresis Cells
- Power Supplies
- Precast Agarose Gels
PowerPac HC
PowerPac Universal
Mini-Sub Cell GT
Wide Mini-Sub Cell GT
39VerniersAnalysis Equipment
- White Light Transilluminator
- BlueView Transilluminator
- White Digital Bioimaging System
- Blue Digital Bioimaging System
White Light Transilluminator
BlueView Transilluminator
White Digital Imaging System
Blue Digital Bioimaging System
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