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LT13 DNA-Profiling and VNTRs

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DNA-profiling and VNTRs and history

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DNA Profiling and Variable Number Tandem Repeats

 DNA profiling techniques take advantage of the many polymorphic sites in human
genomes
Polymorphism = DNA sequence variation that is common in the population – in this
case no single allele is regarded as the standard sequence, instead there are 2 or
ore equally acceptable alternatives
Arbitrary requirement between mutation and polymorphism = the least common
allele must have a frequency of 1% or more in the population. Any lower, the allele is
a mutation
- Polymorphic sequence variants do not normally cause overt debilitating diseases
- Many are found outside genes and have a neutral effect
- Others found within genes but influence characteristics suchs as height, hair
colour etc.
- SNP (single nucleotide polymorphism): contributes to disease susceptibility and
influence drug responses
- Sickle cell allele is polymorphic as it confers resistance to malaria
 By observing the large number of modestly polymorphic sites or a modest number of
highly polymorphic sites – should be able to distinguish differences between each
and every person (except for identical twins)

Mitochondral DNA

 Mitochondral DNA (mtDNA) is moderately
polymorphic and can be used for DNA profiling
 mtDNA particularly useful for forensic identification
where only small amounts o material or only highly
degraded material is available
Due to the fact that the average cell contains
several thousand copies of the mtDNA but only two
copies of nuclear genes
 Somatic cell typically contains 500-1000
mitochondria, an oocyte with 104-105 – mtDNA
immobilised by attachment to IMM clustering into
nucleoids




Y-chromosome

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