Q.33 Which of the following statement(s) about eukaryotic DNA topoisomerase is/are correct? (A) Topoisomerase I creates transient single-strand breaks (B) Topoisomerase I creates transient double-strand breaks (C) Topoisomerase II creates transient single-strand breaks (D) Topoisomerase II creates transient double-strand breaks

Q.33 Which of the following statement(s) about eukaryotic DNA topoisomerase
is/are correct?

(A)
Topoisomerase I creates transient single–strand breaks
(B)
Topoisomerase I creates transient double–strand breaks
(C)
Topoisomerase II creates transient single–strand breaks
(D)
Topoisomerase II creates transient double–strand breaks

Correct answer: (A) and (D)

Eukaryotic DNA topoisomerases manage DNA supercoiling by creating transient breaks, with Type I handling single-strand breaks and Type II managing double-strand breaks.​

Option Analysis

Option A: Correct. Topoisomerase I creates transient single-strand breaks in DNA, forming a covalent bond with the 3′-phosphate end to allow strand rotation and relaxation without ATP.​

Option B: Incorrect. Topoisomerase I does not create double-strand breaks; it specifically targets one strand to relieve torsional stress.​

Option C: Incorrect. Topoisomerase II creates double-strand breaks, not single-strand ones, enabling strand passage between duplexes.​

Option D: Correct. Topoisomerase II introduces transient double-strand breaks, requiring ATP hydrolysis to pass one DNA segment through another before resealing.​

Eukaryotic DNA topoisomerase enzymes are crucial for resolving supercoiling during replication and transcription in CSIR NET Life Sciences topics. These enzymes prevent DNA tangling by creating controlled, transient breaks—single-strand for Topoisomerase I and double-strand for Topoisomerase II—making them high-yield for competitive exams.​

Key Mechanisms

  • Topoisomerase I (Type IB in eukaryotes): Binds duplex DNA, cleaves one strand via transesterification with a tyrosine residue, allows swiveling, then religates. No ATP needed; changes linking number by 1.​

  • Topoisomerase II (Type IIA): Forms a dimeric complex, cleaves both strands (ATP-dependent), passes an intact duplex through the gate, and reseals. Essential for decatenation; changes linking number by 2.​

Exam Relevance

In CSIR NET questions like Q.33, identifying that Topoisomerase I creates transient single-strand breaks (A) and Topoisomerase II creates double-strand breaks (D) scores full marks. Options B and C confuse the types, testing precise knowledge of eukaryotic specifics over prokaryotic (e.g., gyrase).​

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