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首页> 外文期刊>Nucleic Acids Research >Human Rev1 polymerase disrupts G-quadruplex DNA
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Human Rev1 polymerase disrupts G-quadruplex DNA

机译:人Rev1聚合酶破坏G-四链体DNA

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摘要

The Y-family DNA polymerase Rev1 is required for successful replication of G-quadruplex DNA (G4 DNA) in higher eukaryotes. Here we show that human Rev1 (hRev1) disrupts G4 DNA structures and prevents refolding in vitro. Nucleotidyl transfer by hRev1 is not necessary for mechanical unfolding to occur. hRev1 binds G4 DNA substrates with K-d,K-DNA values that are 4-15-fold lower than those of non-G4 DNA substrates. The pre-steady-state rate constant of deoxycytidine monophosphate (dCMP) insertion opposite the first tetrad-guanine by hRev1 is similar to 56% as fast as that observed for non-G4 DNA substrates. Thus, hRev1 can promote fork progression by either dislodging tetrad guanines to unfold the G4 DNA, which could assist in extension by other DNA polymerases, or hRev1 can prevent refolding of G4 DNA structures. The hRev1 mechanism of action against G-quadruplexes helps explain why replication progress is impeded at G4 DNA sites in Rev1-deficient cells and illustrates another unique feature of this enzyme with important implications for genome maintenance.
机译:Y家族DNA聚合酶Rev1是在高级真核生物中成功复制G-四链体DNA(G4 DNA)所必需的。在这里,我们显示人类Rev1(hRev1)破坏了G4 DNA结构,并阻止了体外重折叠。通过hRev1进行的核苷酸转移对于发生机械展开不是必需的。 hRev1以比非G4 DNA底物低4-15倍的K-d,K-DNA值结合G4 DNA底物。 hRev1与第一个四鸟嘌呤相对的单磷酸脱氧胞苷单磷酸酯(dCMP)插入前的稳态速率常数,与非G4 DNA底物观察到的速率常数相似,约为56%。因此,hRev1可以通过去除四联鸟嘌呤以展开G4 DNA来促进叉形前进,这可以帮助其他DNA聚合酶进行延伸,或者hRev1可以阻止G4 DNA结构的重新折叠。 hRev1对抗G-四链体的作用机制有助于解释为什么Rev1缺陷细胞中G4 DNA位点的复制进展受到阻碍,并说明了该酶的另一个独特特征,对基因组的维护具有重要意义。

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