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首页> 外文期刊>Nucleic Acids Research >The mammalian INO80 chromatin remodeling complex is required for replication stress recovery
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The mammalian INO80 chromatin remodeling complex is required for replication stress recovery

机译:复制应力恢复需要哺乳动物Ino80染色质重塑复合物

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摘要

A number of studies have implicated the yeast INO80 chromatin remodeling complex in DNA replication, but the function of the human INO80 complex during S phase remains poorly understood. Here, we have systematically investigated the involvement of the catalytic subunit of the human INO80 complex during unchallenged replication and under replication stress by following the effects of its depletion on cell survival, S-phase checkpoint activation, the fate of individual replication forks, and the consequences of fork collapse. We report that INO80 was specifically needed for efficient replication elongation, while it was not required for initiation of replication. In the absence of the Ino80 protein, cells became hypersensitive to hydroxyurea and displayed hyperactive ATR-Chk1 signaling. Using bulk and fiber labeling of DNA, we found that cells deficient for Ino80 and Arp8 had impaired replication restart after treatment with replication inhibitors and accumulated double-strand breaks as evidenced by the formation of gamma-H2AX and Rad51 foci. These data indicate that under conditions of replication stress mammalian INO80 protects stalled forks from collapsing and allows their subsequent restart.
机译:许多研究涉及DNA复制中的酵母Ino80染色质重塑复合物,但是在S期间的人InO80复合物的功能仍然明显。在这里,我们系统地研究了人Ino80复合物在未经充电的复制期间和复制应力下的催化亚基的累积,通过耗尽对细胞存活,S相检查点激活,单个复制叉的命运的影响,以及叉崩溃的后果。我们报告了有效复制伸长率特别需要INO80,而无需启动复制则是不需要的。在没有INO80蛋白的情况下,细胞对羟基脲保持过敏,并且显示过度ATR-CHK1信号传导。使用DNA的批量和纤维标记,我们发现在用复制抑制剂和累积的双链断膜处理后,INO80和ARP8缺乏的细胞在用复制抑制剂和累积的双链断裂后重新启动,如γ-H2AX和RAD51焦点所证明的。这些数据表明,在复制应力条件下,哺乳动物Ino80保护停滞叉从倒塌,并允许其随后重启。

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