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酿酒酵母Srs2解旋酶在有丝分裂细胞周期、减数分裂及辐照后的调控

Regulation of the Saccharomyces cerevisiae Srs2 helicase during the mitotic cell cycle, meiosis and after irradiation.

作者信息

Heude M, Chanet R, Fabre F

机构信息

Institut Curie, Centre Universitaire, Orsay, France.

出版信息

Mol Gen Genet. 1995 Jul 22;248(1):59-68. doi: 10.1007/BF02456614.

Abstract

The expression of the SRS2 gene, which encodes a DNA helicase involved in DNA repair in Saccharomyces cerevisiae, was studied using an SRS2-lacZ fusion integrated at the chromosomal SRS2 locus. It is shown here that this gene is expressed at a low level and is tightly regulated. It is cell-cycle regulated, with induction probably being coordinated with that of the DNA-synthesis genes, which are transcribed at the G1-S boundary. It is also induced by DNA-damaging agents, but only during the G2 phase of the cell cycle; this distinguishes it from a number of other repair genes, which are inducible throughout the cycle. During meiosis, the expression of SRS2 rises at a time nearly coincident with commitment to recombination. Since srs2 null mutants are radiation sensitive essentially when treated in G1, the mitotic regulation pattern described here leads us to postulate that either secondary regulatory events limit Srs2 activity of G1 cells or Srs2 functions in a repair mechanism associated with replication.

摘要

利用整合在染色体SRS2位点的SRS2 - lacZ融合基因,对编码参与酿酒酵母DNA修复的DNA解旋酶的SRS2基因的表达进行了研究。本文显示该基因低水平表达且受到严格调控。它受细胞周期调控,其诱导可能与在G1 - S边界转录的DNA合成基因的诱导协同进行。它也受DNA损伤剂诱导,但仅在细胞周期的G2期;这使其与许多其他在整个周期均可诱导的修复基因区分开来。在减数分裂过程中,SRS2的表达在与重组起始几乎同时的时间升高。由于srs2缺失突变体在G1期受到处理时基本对辐射敏感,这里描述的有丝分裂调控模式使我们推测,要么二级调控事件限制了G1期细胞的Srs2活性,要么Srs2在与复制相关的修复机制中发挥作用。

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