Dual regulation of Dmc1-driven DNA strand exchange by Swi5-Sfr1 activation and Rad22 inhibition

Both ubiquitously expressed Rad51 and meiosis-specific Dmc1 are required for crossover production during meiotic recombination. The budding yeast Rad52 and its fission yeast ortholog, Rad22, are "mediators;" i.e., they help load Rad51 onto ssDNA coated with replication protein A (RPA). Her...

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Veröffentlicht in:Genes & development 2013-11, Vol.27 (21), p.2299-2304
Hauptverfasser: Murayama, Yasuto, Kurokawa, Yumiko, Tsutsui, Yasuhiro, Iwasaki, Hiroshi
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container_issue 21
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container_title Genes & development
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creator Murayama, Yasuto
Kurokawa, Yumiko
Tsutsui, Yasuhiro
Iwasaki, Hiroshi
description Both ubiquitously expressed Rad51 and meiosis-specific Dmc1 are required for crossover production during meiotic recombination. The budding yeast Rad52 and its fission yeast ortholog, Rad22, are "mediators;" i.e., they help load Rad51 onto ssDNA coated with replication protein A (RPA). Here we show that the Swi5-Sfr1 complex from fission yeast is both a mediator that loads Dmc1 onto ssDNA and a direct "activator" of DNA strand exchange by Dmc1. In stark contrast, Rad22 inhibits Dmc1 action by competing for its binding to RPA-coated ssDNA. Thus, Rad22 plays dual roles in regulating meiotic recombination: activating Rad51 and inhibiting Dmc1.
doi_str_mv 10.1101/gad.218693.113
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subjects Adenosine Triphosphate - metabolism
Crossing Over, Genetic - genetics
DNA Breaks, Double-Stranded
DNA Repair - genetics
DNA, Single-Stranded - metabolism
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Homologous Recombination
Meiosis
Protein Binding
Protein Stability
Rad52 DNA Repair and Recombination Protein - metabolism
Recombinases - metabolism
Research Communication
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins - metabolism
Schizosaccharomyces pombe
Schizosaccharomyces pombe Proteins - genetics
Schizosaccharomyces pombe Proteins - metabolism
title Dual regulation of Dmc1-driven DNA strand exchange by Swi5-Sfr1 activation and Rad22 inhibition
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