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Page 1: Forensic DNA Fingerprinting:  Using Restriction Enzymes

Forensic DNA Fingerprinting: Using Restriction Enzymes

Page 2: Forensic DNA Fingerprinting:  Using Restriction Enzymes

DNA FingerprintingProcedure Overview

Page 3: Forensic DNA Fingerprinting:  Using Restriction Enzymes
Page 4: Forensic DNA Fingerprinting:  Using Restriction Enzymes
Page 5: Forensic DNA Fingerprinting:  Using Restriction Enzymes
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DNA is Tightly Packaged into

Chromosomes Which Reside in the Nucleus

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Model of DNA

DNA is Comprised of Four Base Pairs

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DNA structure

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DNA restriction enzymesEvolved by bacteria to protect against viral DNA infection

Endonucleases = cleave within DNA strands

Over 3,000 known enzymes

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Enzyme Site Recognition • Each enzyme

digests (cuts) DNA at a specific sequence = restriction site

• Enzymes recognize 4- or 6- base pair, palindromic sequences (eg GAATTC)

Palindrome

Restriction site

Fragment 1 Fragment 2

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5 vs 3 Prime Overhang

• Generates 5 prime overhang

Enzyme cuts

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Common Restriction Enzymes

EcoRI– Eschericha coli– 5 prime overhang

Pstl– Providencia stuartii– 3 prime overhang

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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

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DNA Digestion

Temperature

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

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Restriction Fragment Length PolymorphismRFLP

Allele 1

Allele 2

GAATTCGTTAAC

GAATTCGTTAAC

CTGCAGGAGCTC

CGGCAGGCGCTC

PstI EcoRI

1 2 3

3Fragment 1+2Different Base PairsNo restriction site

+

M A-1 A-2

Electrophoresis of restriction fragments

M: MarkerA-1: Allele 1 FragmentsA-2: Allele 2 Fragments

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AgaroseElectrophoresis

Loading

Electrical current carries negatively-charged DNA through gel towards positive (red) electrode

Power Supply

Buffer

Dyes

Agarose gel

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AgaroseElectrophoresis

Running

• Agarose gel sieves DNA fragments according to size

• Small fragments move farther than large fragments

Power Supply

Gel running

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Analysis of Stained Gel

Determinerestriction fragmentsizes

• Create standard curve using DNA marker

• Measure distance traveled by restriction fragments

• Determine size of DNA fragments

Identify the relatedsamples

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Molecular Weight

Determination

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 24.0 100

1,000

10,000

100,000

0 5 10 15 20 25 30

Distance, mm

Size

, bas

e pa

irsB

A

Fingerprinting Standard Curve: Semi-log

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ElectrophoresisEquipment


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