DNA Fingerprinting Using PCR

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DNA Fingerprinting Using PCR. Timothy G. Standish, Ph. D. Polymorphism. Differences between humans can be attributed to two factors: Environmental variation impacting development Individual genes that vary between people These genes which are variable are called polymorphic - PowerPoint PPT Presentation

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©2000 Timothy G. Standish

DNA DNA Fingerprinting Fingerprinting

Using PCRUsing PCRTimothy G. Standish, Ph. D.

©2000 Timothy G. Standish

PolymorphismPolymorphism Differences between humans can be attributed to

two factors:

1. Environmental variation impacting development

2. Individual genes that vary between people These genes which are variable are called

polymorphic Each person is genetically unique because of

their unique set of polymorphic genes All people are related in that the vast majority of

their genes do not vary, but are identical from person to person

©2000 Timothy G. Standish

DNA FingerprintingDNA Fingerprinting DNA fingerprinting involves identification of

DNA segments which vary between individuals A set of DNA fragments polymorphic enough to

provide a unique set of fragments for all individuals, can be used to identify any specific individual in a population

No single fragment will uniquely identify an individual, just as no single polymorphic genetic trait will uniquely identify a person, but a unique set of polymorphic DNA traits/fragments can serve as a reliable means of identification

©2000 Timothy G. Standish

Polymorphism In The TPA GenePolymorphism In The TPA Gene Tissue Plasminogen Activator (TPA) is a

protein that functions in the cascade of reactions which break down blood clots

The gene contains 14 exons and 13 introns Scattered within the introns are 28 Alu

transposon sequences Within intron 8 a single Alu sequence may be

present, or it may be missing Thus, as intron 8 varies with the presence or

absence of Alu, it is polymorphic

©2000 Timothy G. Standish

Polymorphism In The TPA GenePolymorphism In The TPA GeneChromosome 8

Ex11Ex10 Ex13Ex12 Ex14Ex 9Ex 1 Ex 4Ex 3 Ex 6Ex 5 Ex 8Ex 7Ex 2

The TPA Gene13121110987654321

Exon 9Exon 8Intron 8 Intron 9Intron 7

Exon 9Exon 8

ORIntron 8 Intron 9Intron 7

Alu

Polymorphism

©2000 Timothy G. Standish

PCR Detection of TPA PCR Detection of TPA PolymorphismPolymorphism

Reverseprimer

Forwardprimer

960 Base pairsPCR will produce a 660 bp fragment

Exon 9Exon 8

Intron 8

Reverseprimer

Forwardprimer

Alu insertion site

Exon 9Exon 8

ORIntron 8

Alu300 base pairs

660 Base pairsPCR will produce a 660 bp fragment if these primers are used

©2000 Timothy G. Standish

Components of a PCR Components of a PCR ReactionReaction

Buffer (containing Mg++)Template DNA2 Primers that flank the fragment of

DNA to be amplifieddNTPsTaq DNA Polymerase (or another

thermally stable DNA polymerase)

©2000 Timothy G. Standish

PCRPCRMelting

94 oC

Tem

pera

ture

100

0

50

T i m e

5’3’

3’5’

©2000 Timothy G. Standish

PCRPCRMelting

94 oC

Tem

pera

ture

100

0

50

T i m e

3’5’

5’3’

Heat

©2000 Timothy G. Standish

PCRPCRMelting

94 oCAnnealing

Primers50 oC

Extension72 oC

Tem

pera

ture

100

0

50

T i m e

3’5’

5’3’5’

5’

Melting94 oC

©2000 Timothy G. Standish

PCRPCRMelting

94 oCMelting

94 oCAnnealing

Primers50 oC

Extension72 oC

Tem

pera

ture

100

0

50

T i m e

30x

3’5’

5’3’

Heat

Heat

5’

5’

5’

©2000 Timothy G. Standish

PCRPCRMelting

94 oCMelting

94 oCAnnealing

Primers50 oC

Extension72 oC

Tem

pera

ture

100

0

50

T i m e

30x

3’5’

5’3’5’

5’

5’

5’

5’

5’

©2000 Timothy G. Standish

PCRPCRMelting

94 oCMelting

94 oCAnnealing

Primers50 oC

Extension72 oC

Tem

pera

ture

100

0

50

T i m e

30x

3’5’

5’3’ 5’

5’5’

5’

5’

5’

Heat

Heat

©2000 Timothy G. Standish

PCRPCRMelting

94 oCMelting

94 oCAnnealing

Primers50 oC

Extension72 oC

Tem

pera

ture

100

0

50

T i m e

30x

3’5’

5’3’ 5’

5’5’

5’

5’

5’

5’

5’

5’

5’

©2000 Timothy G. Standish

Fragments of defined length

PCRPCRMelting

94 oCMelting

94 oCAnnealing

Primers50 oC

Extension72 oC

Tem

pera

ture

100

0

50

T i m e

30x

3’5’

5’3’ 5’

5’5’

5’

5’

5’

5’

5’

5’

5’

©2000 Timothy G. Standish

DNA Between The Primers Doubles DNA Between The Primers Doubles With Each Thermal CycleWith Each Thermal Cycle

0Cycles

Number1

3

8

2

4

1

2

4

16

5

32

6

64

©2000 Timothy G. Standish

PCR Detection of TPA PCR Detection of TPA PolymorphismPolymorphism

Reverseprimer

Forwardprimer

960 Base pairsPCR will produce a 660 bp fragment

Exon 9Exon 8

Intron 8

Reverseprimer

Forwardprimer

Alu insertion site

Exon 9Exon 8

ORIntron 8

Alu300 base pairs

660 Base pairsPCR will produce a 660 bp fragment if these primers are used

©2000 Timothy G. Standish

Gel ElectrophoresisGel ElectrophoresisHeterozygousHomozygous

with AluHomozygous lacking Alu

©2000 Timothy G. Standish

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