Shuttling along DNA and directed processing of D-loops by RecQ helicase support quality control of homologous recombination

Author:

Harami Gábor M.,Seol Yeonee,In Junghoon,Ferencziová Veronika,Martina Máté,Gyimesi Máté,Sarlós Kata,Kovács Zoltán J.,Nagy Nikolett T.,Sun Yuze,Vellai Tibor,Neuman Keir C.,Kovács Mihály

Abstract

Cells must continuously repair inevitable DNA damage while avoiding the deleterious consequences of imprecise repair. Distinction between legitimate and illegitimate repair processes is thought to be achieved in part through differential recognition and processing of specific noncanonical DNA structures, although the mechanistic basis of discrimination remains poorly defined. Here, we show thatEscherichia coliRecQ, a central DNA recombination and repair enzyme, exhibits differential processing of DNA substrates based on their geometry and structure. Through single-molecule and ensemble biophysical experiments, we elucidate how the conserved domain architecture of RecQ supports geometry-dependent shuttling and directed processing of recombination-intermediate [displacement loop (D-loop)] substrates. Our study shows that these activities together suppress illegitimate recombination in vivo, whereas unregulated duplex unwinding is detrimental for recombination precision. Based on these results, we propose a mechanism through which RecQ helicases achieve recombination precision and efficiency.

Funder

Human Frontier Science Program

Momentum Program of the Hungarian Academy of Sciences

ELTE KMOP

NKFIH

Intramural Research Program of the National Heart, Lung and Blood Institute, NIH

Marie Sklodowska-Curie Reintegration Fellowship

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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