首页> 外文期刊>The Journal of Biochemistry >PCNA mono-ubiquitination and activation of translesion DNA polymerases by DNA polymerase {alpha}.
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PCNA mono-ubiquitination and activation of translesion DNA polymerases by DNA polymerase {alpha}.

机译:PCNA单泛素化和DNA聚合酶{α}激活了病灶DNA聚合酶。

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摘要

Translesion DNA synthesis (TLS) involves PCNA mono-ubiquitination and TLS DNA polymerases (pols). Recent evidence has shown that the mono-ubiquitination is induced not only by DNA damage but also by other factors that induce stalling of the DNA replication fork. We studied the effect of spontaneous DNA replication errors on PCNA mono-ubiquitination and TLS induction. In the pol1L868F strain, which expressed an error-prone pol alpha, PCNA was spontaneously mono-ubiquitinated. Pol alpha L868F had a rate-limiting step at the extension from mismatched primer termini. Electron microscopic observation showed the accumulation of a single-stranded region at the DNA replication fork in yeast cells. For pol alpha errors, pol zeta participated in a generation of +1 frameshifts. Furthermore, in the pol1L868F strain, UV-induced mutations were lower than in the wild-type and a pol delta mutant strain (pol3-5DV), and deletion of the RAD30 gene (pol eta) suppressed this defect. These data suggest that nucleotide misincorporation by pol alpha induces exposure of single-stranded DNA, PCNA mono-ubiquitination and activates TLS pols.
机译:跨病变DNA合成(TLS)涉及PCNA单泛素化和TLS DNA聚合酶(pols)。最近的证据表明,单泛素化不仅是由DNA损伤引起的,而且是由其他引起DNA复制叉停滞的因素引起的。我们研究了自发DNA复制错误对PCNA单泛素化和TLS诱导的影响。在pol1L868F菌株中,它表达容易出错的pol alpha,PCNA自发地被单泛素化。 PolαL868F在错配引物末端延伸时具有限速步骤。电子显微镜观察显示在酵母细胞中DNA复制叉处单链区域的积累。对于pol alpha错误,pol zeta参与了+1移码的生成。此外,在pol1L868F菌株中,紫外线诱导的突变低于野生型和pol delta突变菌株(pol3-5DV),而RAD30基因的缺失(pol eta)抑制了该缺陷。这些数据表明,polα导致的核苷酸错误掺入会诱导单链DNA暴露,PCNA单泛素化并激活TLS pol。

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