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Rad54 and Rdh54 prevent Srs2-mediated disruption of Rad51 presynaptic filaments.
Meir, Aviv; Crickard, J Brooks; Kwon, Youngho; Sung, Patrick; Greene, Eric C.
Afiliação
  • Meir A; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032.
  • Crickard JB; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032.
  • Kwon Y; Department of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Sung P; Department of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Greene EC; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032; ecg2108@cumc.columbia.edu.
Proc Natl Acad Sci U S A ; 119(4)2022 01 25.
Article em En | MEDLINE | ID: mdl-35042797
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Helicases / DNA Topoisomerases / Proteínas de Saccharomyces cerevisiae / Enzimas Reparadoras do DNA Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Helicases / DNA Topoisomerases / Proteínas de Saccharomyces cerevisiae / Enzimas Reparadoras do DNA Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2022 Tipo de documento: Article