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Rad54 and Rdh54 prevent Srs2-mediated disruption of Rad51 presynaptic filaments.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2022 Jan 25; Vol. 119 (4). - Publication Year :
- 2022
-
Abstract
- Srs2 is a superfamily 1 (SF1) helicase that participates in several pathways necessary for the repair of damaged DNA. Srs2 regulates formation of early homologous recombination (HR) intermediates by actively removing the recombinase Rad51 from single-stranded DNA (ssDNA). It is not known whether and how Srs2 itself is down-regulated to allow for timely HR progression. Rad54 and Rdh54 are two closely related superfamily 2 (SF2) motor proteins that promote the formation of Rad51-dependent recombination intermediates. Rad54 and Rdh54 bind tightly to Rad51-ssDNA and act downstream of Srs2, suggesting that they may affect the ability of Srs2 to dismantle Rad51 filaments. Here, we used DNA curtains to determine whether Rad54 and Rdh54 alter the ability of Srs2 to disrupt Rad51 filaments. We show that Rad54 and Rdh54 act synergistically to greatly restrict the antirecombinase activity of Srs2. Our findings suggest that Srs2 may be accorded only a limited time window to act and that Rad54 and Rdh54 fulfill a role of prorecombinogenic licensing factors.<br />Competing Interests: The authors declare no competing interest.<br /> (Copyright © 2022 the Author(s). Published by PNAS.)
- Subjects :
- Cell Cycle Proteins metabolism
DNA Damage physiology
DNA Helicases physiology
DNA Repair genetics
DNA Repair Enzymes genetics
DNA Repair Enzymes physiology
DNA Topoisomerases physiology
DNA, Single-Stranded metabolism
DNA-Binding Proteins metabolism
Homologous Recombination genetics
Protein Binding genetics
Rad51 Recombinase metabolism
Rad51 Recombinase physiology
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae Proteins genetics
Saccharomyces cerevisiae Proteins physiology
DNA Helicases metabolism
DNA Repair Enzymes metabolism
DNA Topoisomerases metabolism
Saccharomyces cerevisiae Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 119
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 35042797
- Full Text :
- https://doi.org/10.1073/pnas.2113871119