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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Mus81 functions in the quality control of replication forks at the rDNA and is involved in the maintenance of rDNA repeat number in Saccharomyces cerevisiae.
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Mus81 functions in the quality control of replication forks at the rDNA and is involved in the maintenance of rDNA repeat number in Saccharomyces cerevisiae.

机译:Mus81在rDNA的复制叉的质量控制中起作用,并参与酿酒酵母中rDNA重复数的维持。

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Previous studies in yeast have suggested that the SGS1 DNA helicase or the Mus81-Mms4 structure-specific endonuclease is required to suppress the accumulation of lethal recombination intermediates during DNA replication. However, the structure of these intermediates and their mechanism of the suppression are unknown. To examine this reaction, we have isolated and characterized a temperature-sensitive (ts) allele of MUS81. At the non-permissive temperature, sgs1Deltamus81(ts) cells arrest at G(2)/M phase after going through S-phase. Bulk DNA replication appears complete but is defective since the Rad53 checkpoint kinase is strongly phosphorylated under these conditions. In addition, the induction of Rad53 hyper-phosphorylation by MMS was deficient at permissive temperature. Analysis of rDNA replication intermediates at the non-permissive temperature revealed elevated pausing of replication forks at the RFB in the sgs1Deltamus81(ts) mutant and a novel linear structure that was dependent on RAD52. Pulsed-field gel electrophoresis of the mus81Delta mutant revealed an expansion of the rDNA locus depending on RAD52, in addition to fragmentation of Chr XII in the sgs1Deltamus81(ts) mutant at permissive temperature. This is the first evidence that Mus81 functions in quality control of replication forks and that it is involved in the maintenance of rDNA repeats in vivo.
机译:酵母中的先前研究表明,需要SGS1 DNA解旋酶或Mus81-Mms4结构特异性核酸内切酶来抑制DNA复制过程中致死重组中间体的积累。但是,这些中间体的结构及其抑制机理尚不清楚。为了检查该反应,我们分离并鉴定了MUS81的温度敏感(ts)等位基因。在非允许温度下,sgs1Deltamus81(ts)细胞在经历S期后停在G(2)/ M期。大量的DNA复制看起来已经完成,但是有缺陷,因为Rad53检查点激酶在这些条件下会被强烈磷酸化。此外,MMS对Rad53过度磷酸化的诱导在允许温度下是不足的。 rDNA复制中间体在非允许温度下的分析显示sgs1Deltamus81(ts)突变体中RFB处复制叉的暂停增加,并且其新型线性结构依赖于RAD52。 mus81Delta突变体的脉冲场凝胶电泳显示,在允许的温度下,除了sgs1Deltamus81(ts)突变体中的Chr XII片段化以外,rDNA基因座还取决于RAD52。这是Mus81在复制叉的质量控制中起作用并且参与体内rDNA重复序列维持的第一个证据。

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