forensics lecture 4- DNA profiling 1 Flashcards

1
Q

what is blood grouping?

A

-Still used in many countries

-Historical cases

-Large samples eliminated by quick inexpensive screening

-Discovery of more systems inherited independently of each other and ABO

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2
Q

what are the problems with blood grouping?

A

-Protein variants – not just blood cell related proteins!

-Quantity of blood may be limited

-Increase typing systems - decrease the number of people sharing the combination

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3
Q

what are biological markers?

A

ABO- AChE (Acetylcholine Esterase)

Rhesus- ACP (Acid Phosphatase)

MNS- Haemoglobin

Kell- PGM (Phosphoglucomutase)

Duffy- G-6-PD Glucose-6-phosphate dehydrogenase

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4
Q

when did DNA profiling begin?

A

1984 – (Sir) Alex Jeffreys
Discovered by chance
First Use – Conviction of Colin Pitchfork

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5
Q

what are secretors?

A

-75 - 85% of population
-Other body fluids have similar profile to serum.
-Higher concentration of A and B antigens

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6
Q

What are identical twins?

A

Have the same DNA
Rosslyn Chapel Rape
Developing technologies - methylation

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7
Q

Methodology - RFLP v PCR of STRs…

A

RFLP (Restriction Fragment length polymorphism) Analysis
Variable number tandem repeats
Large amounts of DNA required
Requires undegraded material (warm moist conditions increase degradation)

PCR (Polymerase Chain reaction) of STRs ( Short tandem repeats)
Less DNA required
Can be partially degraded

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8
Q

what is mitochondrial DNA?

A

-1 mitochondrion has 5-10 identical circular molecules of DNA
-Each 16569 base pairs – 37 genes
-Useful in mass disasters to link family members.

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9
Q

what are the odds ratios of each blood group?

A

Odds ratio of each blood group (UK)

O+	   	1/3
O-	   	1/15
A+	   	1/3
A-	   	1/16
B+	   	1/12
B-	   	1/67
AB+ 		1/29
AB-  	1/167
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10
Q

what are good and bad sources of DNA?

A

good = blood, sperm, ovum, hair

bad = skin cells, faeces, hair shaft, urine

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