首页> 外文期刊>Nucleic Acids Research >End-bridging is required for pol mu to efficiently promote repair of noncomplementary ends by nonhomologous end joining
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End-bridging is required for pol mu to efficiently promote repair of noncomplementary ends by nonhomologous end joining

机译:pol需要末端桥接,以通过非同源末端连接有效地促进非互补末端的修复

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摘要

DNA polymerase mu is a member of the mammalian pol X family and reduces deletion during chromosome break repair by nonhomologous end joining (NHEJ). This biological role is linked to pol mu's ability to promote NHEJ of ends with noncomplementary 3' overhangs, but questions remain regarding how it performs this role. We show here that synthesis by pol mu in this context is often rapid and, despite the absence of primer/template base-pairing, instructed by template. However, pol mu is both much less active and more prone to possible template independence in some contexts, including ends with overhangs longer than two nucleotides. Reduced activity on longer overhangs implies pol mu is less able to synthesize across longer gaps, arguing pol mu must bridge both sides of gaps between noncomplementary ends to be effective in NHEJ. Consistent with this argument, a pol mu mutant defective specifically on gapped substrates is also less active during NHEJ of noncomplementary ends both in vitro and in cells. Taken together, pol mu activity during NHEJ of noncomplementary ends can thus be primarily linked to pol mu's ability to work together with core NHEJ factors to bridge DNA ends and perform a template-dependent gap fill-in reaction.
机译:DNA聚合酶mu是哺乳动物pol X家族的成员,可通过非同源末端连接(NHEJ)减少染色体断裂修复过程中的缺失。这种生物学作用与pol mu促进具有非互补3'突出端的末端NHEJ的能力有关,但有关其如何发挥此作用的问题仍然存在。我们在这里显示,在这种情况下,通过pol mu进行的合成通常是快速的,尽管没有引物/模板碱基配对,但仍受模板指示。但是,在某些情况下,pol mu的活性不仅低得多,而且更可能具有模板独立性,包括突出端长于两个核苷酸的末端。在较长的突出端上活性的降低意味着聚合酶不能在较长的缺口中合成,认为聚合酶必须桥接非互补末端之间的缺口的两侧以在NHEJ中有效。与该论点一致,在体外和细胞中非互补末端的NHEJ期间,特异在空位基质上缺陷的pol mu突变体的活性也较低。两者合计,非互补末端NHEJ期间的pol mu活性因此可以主要与pol mu与核心NHEJ因子共同作用以桥接DNA末端并进行模板依赖性缺口填充反应的能力有关。

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