Kalvi.NEET

Frameshift Mutation

சட்டக இடப்பெயர்ச்சி சடுதிமாற்றம்

NCERT Class 12 · Molecular Basis of Inheritance · 2 NEET questions

A single base pair shift is not a minor error; it is a catastrophic rewrite of the genetic code. If you think the ribosome ignores a single missing nucleotide, you are failing the exam. Biology is digital, not analog.

The idea

Frameshift mutation occurs due to the insertion or deletion of one or two base pairs in the DNA sequence. This alters the reading frame from the point of mutation, resulting in a completely different sequence of amino acids. However, the insertion or deletion of three or its multiples of bases adds or removes one or more codons, leaving the reading frame downstream unaltered.

Why it matters

It is a consequence of errors in DNA replication or damage, demonstrating the necessity of the triplet reading frame for correct protein synthesis.

NEET lens

NEET focuses on the 'multiple of three' rule. Expect questions asking whether a specific mutation alters the reading frame or just adds/removes an amino acid. Do not confuse point mutation with frameshift mutation. Memorize that 3-base changes preserve the frame; 1 or 2-base changes destroy it.

Clinical significance

Frameshift mutations are the primary cause of Duchenne Muscular Dystrophy and Tay-Sachs disease. These mutations lead to the production of non-functional, truncated proteins that fail to perform essential cellular tasks. The body cannot compensate for such fundamental errors in translation.

Introduction

A frameshift mutation is the insertion or deletion of one or two bases in a gene, which changes the reading frame from that point onwards.

Core concept

Because codons are read contiguously in triplets, adding or deleting one or two bases shifts every following codon, so the amino acid sequence after the mutation changes completely (and often a premature stop codon appears). Inserting or deleting three bases (or multiples of three) adds or removes one (or more) amino acids but keeps the reading frame from that point onwards. Point mutation = change in a single base pair (e.g. sickle-cell anaemia: GAG → GUG, Glu → Val at the 6th position of the beta-globin chain).

Go deeper

Classic sentence example: RAM HAS RED CAP → delete one letter → RAM ASR EDC AP (meaningless); delete three letters → RAM RED CAP (still meaningful, just shorter).

From Class 10

Imagine a sentence of three-letter words. Remove one letter and every word after it becomes nonsense — that is a frameshift.

Previous year NEET questions (2)

  1. NEET 2019

    Under which of the following conditions will there be no change in the reading frame of following mRNA? 5'AACAGCGGUGCUAUU3'

    1. Insertion of G at 5th position
    2. Deletion of G from 5th position
    3. Insertion of A and G at 4th and 5th positions respectively
    4. Deletion of GGU from 7th, 8th and 9th positions
    Show answer

    Answer: (D) Deletion of GGU from 7th, 8th and 9th positions

  2. NEET 2017

    If there are 999 bases in an RNA that codes 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?

    1. 1
    2. 11
    3. 33
    4. 333
    Show answer

    Answer: (C) 33

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