RNase h2缺陷细胞中自发重组的增加是由多个连续的rNMP引起的,而不是由DNA聚合酶epsilon结合的单个rNMP残基引起的

IF 4.1 3区 生物学 Q2 CELL BIOLOGY
Anastasiya Epshtein, Catherine J. Potenski, H. Klein
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引用次数: 18

摘要

由于DNA聚合酶的插入、无法移除冈崎片段引物、启动复制的r环以及RNA/ cdna介导的重组,核糖核苷酸可以嵌入DNA中。RNA:DNA杂交体被RNase H酶去除。DNA中的单个rNMPs被RNase H2去除,如果它们留在前导链上,可以通过top1依赖性途径导致突变。DNA中的rNMPs也可以刺激基因组的不稳定性,其中包括同源重组基因转换事件。我们之前发现,与rnmp刺激的诱变类似,rnmp刺激的重组也是依赖于top1的。然而,与诱变不同的是,我们在这里报告了由复制聚合酶epsilon结合的rNMPs不会刺激重组。相反,重组似乎是由多个连续的rnmp刺激的,这可能是由r环或复制启动事件引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increased spontaneous recombination in RNase H2-deficient cells arises from multiple contiguous rNMPs and not from single rNMP residues incorporated by DNA polymerase epsilon
Ribonucleotides can become embedded in DNA from insertion by DNA polymerases, failure to remove Okazaki fragment primers, R-loops that can prime replication, and RNA/cDNA-mediated recombination. RNA:DNA hybrids are removed by RNase H enzymes. Single rNMPs in DNA are removed by RNase H2 and if they remain on the leading strand, can lead to mutagenesis in a Top1-dependent pathway. rNMPs in DNA can also stimulate genome instability, among which are homologous recombination gene conversion events. We previously found that, similar to the rNMP-stimulated mutagenesis, rNMP-stimulated recombination was also Top1-dependent. However, in contrast to mutagenesis, we report here that recombination is not stimulated by rNMPs incorporated by the replicative polymerase epsilon. Instead, recombination seems to be stimulated by multiple contiguous rNMPs, which may arise from R-loops or replication priming events.
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来源期刊
Microbial Cell
Microbial Cell Multiple-
CiteScore
6.40
自引率
0.00%
发文量
32
审稿时长
12 weeks
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