首页> 外文OA文献 >Double-strand break repair in the absence of RAD51 in yeast: a possible role for break-induced DNA replication.
【2h】

Double-strand break repair in the absence of RAD51 in yeast: a possible role for break-induced DNA replication.

机译:酵母中不存在RAD51的双链断裂修复:断裂诱导的DNA复制的可能作用。

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

In wild-type diploid cells of Saccharomyces cerevisiae, an HO endonuclease-induced double-strand break (DSB) at the MAT locus can be efficiently repaired by gene conversion using the homologous chromosome sequences. Repair of the broken chromosome was nearly eliminated in rad52delta diploids; 99% lost the broken chromosome. However, in rad51delta diploids, the broken chromosomes were repaired approximately 35% of the time. None of these repair events were simple gene conversions or gene conversions with an associated crossover, instead, they created diploids homozygous for the MAT locus and all markers in the 100-kb region distal to the site of the DSB. In rad51delta diploids, the broken chromosome can apparently be inherited for several generations, as many of these repair events are found as sectored colonies, with one part being repaired and the other part being lost the broken chromosome. Similar events occur in about 2% of wild-type cells. We propose that a broken chromosome end can invade a homologous template in the absence of RAD51 and initiate DNA replication that may extend to the telomere, 100 or more kb away. Such break-induced replication appears to be similar to recombination-initiated replication in bacteria.
机译:在酿酒酵母的野生型二倍体细胞中,可以通过使用同源染色体序列进行基因转化来有效修复MAT基因座处的HO内切核酸酶诱导的双链断裂(DSB)。 rad52delta二倍体几乎消除了断裂染色体的修复; 99%的染色体丢失了。但是,在rad51delta二倍体中,大约35%的时间修复了断裂的染色体。这些修复事件均不是简单的基因转换或具有相关交叉的基因转换,而是它们为MAT基因座和DSB末端远端100 KB区域中的所有标记纯合了二倍体。在rad51delta二倍体中,断裂的染色体显然可以遗传数代,因为其中许多修复事件都是扇形集落,一部分被修复,另一部分丢失了断裂的染色体。类似事件发生在约2%的野生型细胞中。我们提出,在没有RAD51的情况下,断裂的染色体末端可以侵入同源模板,并启动DNA复制,该复制可能延伸至100 kb或更多kb的端粒。这种断裂诱导的复制似乎与细菌中重组起始的复制相似。

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