Rad54 and Rdh54 prevent Srs2-mediated disruption of Rad51 presynaptic filaments

被引:9
作者
Meir, Aviv [1 ]
Crickard, J. Brooks [1 ,3 ]
Kwon, Youngho [2 ]
Sung, Patrick [2 ]
Greene, Eric C. [1 ]
机构
[1] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem & Struct Biol, San Antonio, TX 78229 USA
[3] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
关键词
Rad51; Srs2; Rad54; Rdh54; homologous recombination; SINGLE-STRANDED-DNA; SACCHAROMYCES-CEREVISIAE; HOMOLOGOUS RECOMBINATION; YEAST RAD51; DUPLEX DNA; SRS2; PROTEIN; REPAIR; DISSOCIATION; MUTATIONS;
D O I
10.1073/pnas.2113871119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 abil-ity of Srs2 to dismantle Rad51 filaments. Here, we used DNA cur-tains 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 lim-ited time window to act and that Rad54 and Rdh54 fulfill a role of prorecombinogenic licensing factors.
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页数:10
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