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复制后黏连的形成是修复所必需的,且由单个DNA断裂诱导产生。

Postreplicative formation of cohesion is required for repair and induced by a single DNA break.

作者信息

Ström Lena, Karlsson Charlotte, Lindroos Hanna Betts, Wedahl Sara, Katou Yuki, Shirahige Katsuhiko, Sjögren Camilla

机构信息

Department of Cell and Molecular Biology, Karolinska Institute, 171 77 Stockholm, Sweden.

出版信息

Science. 2007 Jul 13;317(5835):242-5. doi: 10.1126/science.1140649.

Abstract

Sister-chromatid cohesion, established during replication by the protein complex cohesin, is essential for both chromosome segregation and double-strand break (DSB) repair. Normally, cohesion formation is strictly limited to the S phase of the cell cycle, but DSBs can trigger cohesion also after DNA replication has been completed. The function of this damage-induced cohesion remains unknown. In this investigation, we show that damage-induced cohesion is essential for repair in postreplicative cells in yeast. Furthermore, it is established genome-wide after induction of a single DSB, and it is controlled by the DNA damage response and cohesin-regulating factors. We thus define a cohesion establishment pathway that is independent of DNA duplication and acts together with cohesion formed during replication in sister chromatid-based DSB repair.

摘要

姐妹染色单体黏连在复制过程中由蛋白质复合体黏连蛋白建立,对染色体分离和双链断裂(DSB)修复都至关重要。正常情况下,黏连的形成严格限于细胞周期的S期,但DSB在DNA复制完成后也能触发黏连。这种损伤诱导的黏连的功能尚不清楚。在本研究中,我们表明损伤诱导的黏连对酵母复制后细胞的修复至关重要。此外,在单个DSB诱导后全基因组范围内都会建立这种黏连,并且它受DNA损伤反应和黏连蛋白调节因子的控制。因此,我们定义了一条黏连建立途径,该途径独立于DNA复制,并在基于姐妹染色单体的DSB修复中与复制过程中形成的黏连共同起作用。

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