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首页> 外文期刊>Science Advances >Phosphoregulation of Rad51/Rad52 by CDK1 functions as a molecular switch for cell cycle–specific activation of homologous recombination
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Phosphoregulation of Rad51/Rad52 by CDK1 functions as a molecular switch for cell cycle–specific activation of homologous recombination

机译:CDK1通过CDK1的Rad51 / Rad52的磷酸化用作用于细胞周期的同源重组的特异性活化的分子开关

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Homologous recombination is exquisitely activated only during specific cell phases. In the G 1 phase, homologous recombination activity is completely suppressed. According to previous reports, the activation of homologous recombination during specific cell phases depends on the kinase activity of cyclin-dependent kinase 1 (CDK1). However, the precise regulatory mechanism and target substrates of CDK1 for this regulation have not been completely determined. Here, we report that the budding yeast CDK1, Cdc28, phosphorylates the major homologous recombination regulators Rad51 and Rad52. This phosphorylation occurs in the G 2 /M phase by Cdc28 in combination with G 2 /M phase cyclins. Nonphosphorylatable mutations in Rad51 and Rad52 impair the DNA binding affinity of Rad51 and the affinity between Rad52 rings that leads to their interaction. Collectively, our data provide detailed insights into the regulatory mechanism of cell cycle–dependent homologous recombination activation in eukaryotic cells.
机译:在特定的细胞相期间仅在特定的细胞相期间被激活同源重组。在G 1相中,完全抑制同源重组活性。根据先前的报道,特定细胞相期间同源重组的激活取决于细胞周期蛋白依赖性激酶1(CDK1)的激酶活性。然而,该调节的精确调节机制和CDK1的靶底物尚未完全确定。在这里,我们报告说,萌芽酵母CDK1,CDC28,磷酸化主要同源重组调节器RAD51和RAD52。通过CDC28与G 2 / M相色调组合的G 2 / M相发生这种磷酸化。 RAD51和RAD52中的非磷属可释放突变损害RAD51的DNA结合亲和力,并导致其相互作用的RAD52环之间的亲和力。统称,我们的数据提供了详细的见解,进入真核细胞中细胞周期依赖性同源重组活化的调节机制。

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