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TRESLIN-MTBP 复合物将 DNA 复制完成与 S/G2 期转换偶联。

The TRESLIN-MTBP complex couples completion of DNA replication with S/G2 transition.

机构信息

Center for Chromosome Stability, Institute for Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200, Denmark.

Max Delbrück Center for Molecular Medicine (MDC), 13092 Berlin, Germany; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200, Denmark.

出版信息

Mol Cell. 2022 Sep 15;82(18):3350-3365.e7. doi: 10.1016/j.molcel.2022.08.006. Epub 2022 Aug 31.

Abstract

It has been proposed that ATR kinase senses the completion of DNA replication to initiate the S/G2 transition. In contrast to this model, we show here that the TRESLIN-MTBP complex prevents a premature entry into G2 from early S-phase independently of ATR/CHK1 kinases. TRESLIN-MTBP acts transiently at pre-replication complexes (preRCs) to initiate origin firing and is released after the subsequent recruitment of CDC45. This dynamic behavior of TRESLIN-MTBP implements a monitoring system that checks the activation of replication forks and senses the rate of origin firing to prevent the entry into G2. This system detects the decline in the number of origins of replication that naturally occurs in very late S, which is the signature that cells use to determine the completion of DNA replication and permit the S/G2 transition. Our work introduces TRESLIN-MTBP as a key player in cell-cycle control independent of canonical checkpoints.

摘要

有人提出,ATR 激酶感知 DNA 复制的完成,以启动 S/G2 期转换。与该模型相反,我们在这里表明,TRESLIN-MTBP 复合物在 ATR/CHK1 激酶的独立作用下,防止过早地从早期 S 期进入 G2 期。TRESLIN-MTBP 在复制前复合物 (preRC) 上短暂作用,启动起始原点的引发,然后在随后 CDC45 的招募后释放。TRESLIN-MTBP 的这种动态行为实现了一个监控系统,该系统检查复制叉的激活情况,并感知起始原点引发的速度,以防止进入 G2 期。该系统检测到在非常晚的 S 期自然发生的复制原点数量的减少,这是细胞用来确定 DNA 复制完成并允许 S/G2 期转换的标志。我们的工作引入了 TRESLIN-MTBP,作为独立于经典检测点的细胞周期控制的关键参与者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/378d/9506001/367b1701f0d4/fx1.jpg

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