首页> 美国卫生研究院文献>Cell Cycle >Homologous chromosomes move and rapidly initiate contact at the sites of double-strand breaks in genes in G₀-phase human cells
【2h】

Homologous chromosomes move and rapidly initiate contact at the sites of double-strand breaks in genes in G₀-phase human cells

机译:同源染色体移动并快速启动G₀期人类细胞基因双链断裂位点的接触

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We recently reported that homologous chromosomes make contact at the sites of double-strand breaks (DSBs) induced by ionizing radiation (IR) and the restriction endonuclease I-PpoI in G₀/G₁-phase somatic human cells. The contact involves short segments of homologous chromosomes and is centered on a DSB that occurs in a gene; contact does not occur at a DSB in intergenic DNA. Contact between homologous chromosomes is abrogated by inhibition of transcription and requires the kinase activity of ATM, but not DNA-PK. Here, we report additional insights into the mechanism underlying this novel phenomenon. We identify four patterns of homologous chromosome contact, and show that contact between homologous arms, but not centrosomes, is induced by IR. Significantly, we demonstrate that contact is induced by IR in non-proliferating, G₀-phase human cells derived from tissue explants. Finally, we show that contact between homologous chromosomes is detectable as early as 5 min after IR. These results point to the existence of a mechanism that rapidly localizes homologous chromosome arms at sites of DSBs in genes in G₀-phase human cells.
机译:我们最近报道,同源染色体在电离辐射(IR)和限制性核酸内切酶I-PpoI诱导的双链断裂(DSBs)的位点接触,G / G相处于体细胞中。接触涉及同源染色体的短片段,并以基因中存在的DSB为中心。基因DNA中的DSB不会发生接触。同源染色体之间的接触通过抑制转录而被废除,并且需要ATM的激酶活性,而不需要DNA-PK。在这里,我们报告有关这种新现象的潜在机制的其他见解。我们确定同源染色体接触的四种模式,并表明同源臂之间,但不是中心体之间的接触是由红外诱导的。重要的是,我们证明了接触是由IR诱导的来自组织外植体的非增殖性G 1期人细胞。最后,我们显示同源染色体之间的接触最早可在IR后5分钟检测到。这些结果表明存在一种将同源染色体臂迅速定位在G 1期人类细胞基因中DSBs位点上的机制的存在。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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