- 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 iiiColumn X terms
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A. Random mutagenesis – mutations introduced at unpredictable sites across the genome.
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B. Targeted mutagenesis – precise changes at a known locus.
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C. Phenocopying – imitating a mutant phenotype without changing DNA sequence (usually transient gene knock‑down).
Column Y strategies
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i. RNAi – sequence‑specific mRNA degradation → transient loss‑of‑function phenotype.
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ii. Transposable elements – random insertion into genome causing insertional mutations.
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iii. Homologous recombination – gene targeting at a defined locus.
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iv. UV mutagenesis – random DNA damage and mutations genome‑wide.
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v. CRISPR – programmable, highly site‑specific genome editing.
Correct matches
A. Random mutagenesis → ii (Transposable elements) and iv (UV mutagenesis)
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UV light causes random point mutations and small lesions across the genome.
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Transposable elements insert more or less randomly, disrupting genes.
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Both are classic tools for random mutagenesis.
B. Targeted mutagenesis → iii (Homologous recombination) and v (CRISPR)
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Homologous recombination with a designed donor construct enables gene targeting at a specific locus.
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CRISPR–Cas systems use a guide RNA to direct cuts at defined sequences, enabling precise knockouts or edits.
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Both therefore mediate targeted mutagenesis.
C. Phenocopying → i (RNAi)
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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:
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A – ii & iv
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B – iii & v
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C – i
which corresponds to option (1).
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