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प्रश्न
Frame shift mutations occur following:
पर्याय
tautomeric shifts
base substitutions
dimer formation
insertion/deletion of single base
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उत्तर
insertion/deletion of single base
Explanation:
Frame shift mutations occur when there is an insertion or deletion of a single nucleotide base in the DNA sequence. Because the genetic code is read in triplets (codons), adding or removing a base shifts the reading frame from that point onward, altering the entire amino acid sequence downstream. This often results in a completely different and usually nonfunctional protein. Tautomeric shifts, base substitutions, or dimer formation generally cause other types of mutations but do not cause a frame shift. Hence, frame shift mutations specifically follow insertion or deletion of a base.
