13. The following table enlists different ways of carrying out reverse genetics (Column X) and different strategies to achieve the same (Column Y) Which one of the following options is a correct match between Column X and Y? (1) A - i and iv; B - iii; C - ii and v (2) A - ii and iv; B - iii and v (3) A- i and iv; B - iii and v (4) A - ii and iv; B - i and iii
  1. The following table enlists different ways of carrying out reverse genetics (Column X) and different strategies to achieve the same (Column Y)

    Which one of the following options is a correct match between Column X and Y?
    (1) A – i and iv; B – iii; C – ii and v
    (2) A – ii and iv; B – iii and v
    (3) A- i and iv; B – iii and v
    (4) A – ii and iv; B – i and iii

    Column X terms

    • A. Random mutagenesis – mutations introduced at unpredictable sites across the genome.

    • B. Targeted mutagenesis – precise changes at a known locus.

    • C. Phenocopying – imitating a mutant phenotype without changing DNA sequence (usually transient gene knock‑down).

    Column Y strategies

    • i. RNAi – sequence‑specific mRNA degradation → transient loss‑of‑function phenotype.

    • ii. Transposable elements – random insertion into genome causing insertional mutations.

    • iii. Homologous recombination – gene targeting at a defined locus.

    • iv. UV mutagenesis – random DNA damage and mutations genome‑wide.

    • v. CRISPR – programmable, highly site‑specific genome editing.


    Correct matches

    A. Random mutagenesis → ii (Transposable elements) and iv (UV mutagenesis)

    • UV light causes random point mutations and small lesions across the genome.

    • Transposable elements insert more or less randomly, disrupting genes.

    • Both are classic tools for random mutagenesis.

    B. Targeted mutagenesis → iii (Homologous recombination) and v (CRISPR)

    • Homologous recombination with a designed donor construct enables gene targeting at a specific locus.

    • CRISPR–Cas systems use a guide RNA to direct cuts at defined sequences, enabling precise knockouts or edits.

    • Both therefore mediate targeted mutagenesis.

    C. Phenocopying → i (RNAi)

    • RNA interference knocks down mRNA, creating a reversible, non‑genomic loss‑of‑function phenotype, i.e., a phenocopy of a knockout.

    So the full correct pattern is:

    • A – ii & iv

    • B – iii & v

    • C – i

    which corresponds to option (1).

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