What is it that forms the basis of $DNA$ fingerprinting ?
AIPMT 2012, Medium
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d (d) : $DNA$ fingerprinting is a technique of determining nucleotide sequences of certain areas of $DNA$ which are unique to each individual. The difference of about $0.1\%$ or $3 × 10^6$ base pairs (out of $3 × 10^9\ bp$) provides individuality to each human being. Human genome possesses numerous small noncoding but inheritable sequences of bases which are repeated many times. These sequences occur near telomere, centromeres, $Y$ chromosome and heterochromatic area. The area with same sequence of bases repeated several times is called repetitive $DNA$. It is separated as satellite from the bulk $DNA$ during density gradient centrifugation and hence called satellite $DNA$ where, repetition of bases is in tandem. Satellite $DNAs$ show polymorphism (the occurrence of mutations in a population at high frequency), which is the basis of genetic mapping of human genome as well as $DNA$ fingerprinting. While mutations in genes produce alleles with different expressions, mutations in noncoding repetitive $DNA$ have no immediate impact. These mutations which have piled up with time form the basis of polymorphism.
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$A$ : Unknown $DNA$ after hybridization with $VNTR$ probe, the autoradiogram gives many bands of differing sizes in $DNA$ profiling.
$R$ : These bands represents $DNA$ fingerprint of organism
If there are $999$ bases in an $RNA$ that code for a protein with $333$ amino acids, and the base at position $901$ is deleted such that the length of the $RNA$ becomes $998$ bases, how many codons will be altered?