what is DNA fingerprinting?

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DNA fingerprinting is a way of identifying a specific individual, rather than simply identifying a species or some particular trait. It is also known as genetic fingerprinting or DNA profiling. As a technology, it has been around since at least 1985, when it was announced by its inventor, Sir Alec Jeffrey. DNA fingerprinting is currently used both for identifying paternity or maternity and for identifying criminals or victims. There is discussion of using DNA fingerprinting as a sort of personal identifier as well, although the viability of this is debatable.

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I am providing an image which describes the process of DNA fingerprinting in details. Actually VNTRs are the markers and southern blot is a technique to identify those markers.

 

Hope this clears your doubt!!

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DNA fingerprinting is a method for comparing the DNA sequences of any two individuals. Repetitive DNA is separated from bulk genomic DNA since it appears as a distinct peak during density gradient centrifugation. Satellites are of two types—micro-satellites and mini satellites, depending upon the base composition, length of segment and the number of repetitive units.

Satellites do not code for proteins, but have a major role to play in DNA fingerprinting.

Polymorphism is actually a result of mutation. A germ cell mutation (which can pass on to the next generation through sexual reproduction) gives rise to polymorphism in populations.

In other words, an inheritable mutation if observed in higher frequencies in a population is known as polymorphism. Polymorphisms arise normally in non-coding sequences because mutations in non-coding sequences do not affect an individual’s reproductive ability.

VNTR ( variable number of tandem repeats) are satellite DNAs that show high degree of polymorphism. VNTRs are used as probes in DNA fingerprinting.

First of all, DNA from an individual is isolated and cut with restriction endonucleases. Fragments are separated according to their size and molecular weight on gel electrophoresis. Fragments separated on electrophoresis gel are blotted (immobilised) on a synthetic membrane such as nylon or nitrocellulose. Immobilised fragments are hybridised with a VNTR probe. Hybridised DNA fragments can be detected by autoradiography. VNTRs vary in size from 0.1 to 20 kb. Hence, in the autoradiogram, band of different sizes will be obtained. These bands are characteristic for an individual. They are different in each individual, except identical twins.

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