(A) Deaminating agent
(B) Alkylating agent
(C) Intercalating agent
(D) Base analogue
Ethidium bromide is a classic intercalating agent used in molecular biology labs. This article covers Q.48 on its mutagenic action with the correct answer and breakdowns of all options.
Correct Answer
The correct answer is (C) Intercalating agent.
Ethidium bromide (EtBr) features a flat, planar ring structure that slips between DNA base pairs, known as intercalation. This distorts the DNA helix, unwinds it, and disrupts replication, transcription, and repair, causing frameshift mutations.
Option Breakdowns
(A) Deaminating Agent
Deaminating agents like nitrous acid remove amino groups from bases (e.g., cytosine to uracil), leading to base mismatches.
Ethidium bromide does not deaminate; it physically inserts into DNA stacks instead.
(B) Alkylating Agent
Alkylating agents such as mustard gas add alkyl groups to DNA bases, causing cross-links or breaks.
EtBr lacks this chemical reactivity; its effect is structural insertion, not covalent modification.
(C) Intercalating Agent
EtBr intercalates between base pairs due to its phenanthridine ring, increasing DNA length by ~26% per molecule.
This interference induces mutations, explaining its use (and hazard) in DNA visualization via gel electrophoresis.
(D) Base Analogue
Base analogues like 5-bromouracil mimic nucleotides and pair erroneously during replication.
EtBr does not incorporate as a base; it binds externally between existing pairs.
| Option | Mechanism | Mutation Type | Matches EtBr? |
|---|---|---|---|
| (A) Deaminating | Removes NH₂ from bases | Transitions | No |
| (B) Alkylating | Adds alkyl groups | Cross-links | No |
| (C) Intercalating | Inserts between bases | Frameshifts | Yes |
| (D) Base Analogue | Mimics nucleotides | Mispairing | No |