...
【24h】

Fork pausing complex engages topoisomerases at the replisome

机译:叉暂停复合物在普罗基替换物中啮合

获取原文
获取原文并翻译 | 示例
           

摘要

Replication forks temporarily or terminally pause at hundreds of hard-to-replicate regions around the genome. A conserved pair of budding yeast replisome components Tof1-Csm3 (fission yeast Swi1-Swi3 and human TIME-LESS-TIPIN) act as a "molecular brake" and promote fork slowdown at proteinaceous replication fork barriers (RFBs), while the accessory helicase Rrm3 assists the replisome in removing protein obstacles. Here we show that the Tof1-Csm3 complex promotes fork pausing independently of Rrm3 helicase by recruiting topoisomerase I (Top1) to the replisome. Topoisomerase II (Top2) partially compensates for the pausing decrease in cells when Top1 is lost from the replisome. The C terminus of Tof1 is specifically required for Top1 recruitment to the replisome and fork pausing but not for DNA replication checkpoint (DRC) activation. We propose that forks pause at proteinaceous RFBs through a "sTOP" mechanism ("slowing down with topoisomerases I-II"), which we show also contributes to protecting cells from topoisomerase-blocking agents.
机译:Replication Forks临时或终止暂停在基因组周围数百个难以复制的区域。保守的一对萌芽酵母典型成分TOF1-CSM3(裂变酵母SWI1-SWI3和人的时间 - 少量钢丝)作为“分子制动器”,促进蛋白质复制叉屏障(RFBS)的叉子放缓,而配件螺旋酶RRM3协助重写蛋白质障碍物。在这里,我们表明TOF1-CSM3复合物通过募集TOPOISOMERASE I(TOP1)促进RRM3螺旋酶的叉暂停。拓扑异构酶II(TOP2)部分补偿当TOP1从替换物中丢失时细胞的暂停减少。 TOF1的C末端是TOP1募集到额外的丢失,但不用于DNA复制检查点(DRC)激活。我们提出叉子在蛋白质RFBS通过“止止”机制暂停(用拓扑异构酶I-II速度减慢),我们表明我们还有助于保护来自拓扑异构酶阻断剂的细胞。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号