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Direct observation of helicase–topoisomerase coupling within reverse gyrase.

Authors :
Xi Yang
Garnier, Florence
Débat, Hélène
Strick, Terence R.
Nadal, Marc
Neuman, Keir C.
Source :
Proceedings of the National Academy of Sciences of the United States of America. 5/19/2020, Vol. 117 Issue 20, p1-9. 9p.
Publication Year :
2020

Abstract

Reverse gyrases (RGs) are the only topoisomerases capable of generating positive supercoils in DNA. Members of the type IA family, they do so by generating a single-strand break in substrate DNA and then manipulating the two single strands to generate positive topology. Here, we use single-molecule experimentation to reveal the obligatory succession of steps that make up the catalytic cycle of RG. In the initial state, RG binds to DNA and unwinds ∼2 turns of the double helix in an ATP-independent fashion. Upon nucleotide binding, RG then rewinds ∼1 turn of DNA. Nucleotide hydrolysis and/or product release leads to an increase of 2 units of DNA writhe and resetting of the enzyme, for a net change of topology of +1 turn per cycle. Final dissociation of RG from DNA results in rewinding of the 2 turns of DNA that were initially disrupted. These results show how tight coupling of the helicase and topoisomerase activities allows for induction of positive supercoiling despite opposing torque. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
117
Issue :
20
Database :
Academic Search Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
143351016
Full Text :
https://doi.org/10.1073/pnas.1921848117