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A euryarchaeal histone modulates strand displacement synthesis by replicative DNA polymerases

机译:euryarchaeal组蛋白通过复制性DNA聚合酶调节链置换合成

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Euryarchaeota and Crenarchaeota, the two main lineages of the domain Archaea, encode different chromatin proteins and differ in the use of replicative DNA polymerases. Crenarchaea possess a single family B DNA polymerase (PolB), which is capable of strand displacement modulated by the chromatin proteins Cren7 and Sul7d. Euryarchaea have two distinct replicative DNA polymerases, PolB and PolD, a family D DNA polymerase. Here we characterized the strand displacement activities of PolB and PolD from the hyperthermophilic euryarchaeon Pyrococcus furiosus and investigated the influence of HPfA1, a homolog of eukaryotic histones from P. furiosus , on these activities. We showed that both PolB and PolD were efficient in strand displacement. HPfA1 inhibited DNA strand displacement by both DNA polymerases but exhibited little effect on the displacement of a RNA strand annealed to single-stranded template DNA. This is consistent with the finding that HPfA1 bound more tightly to double-stranded DNA than to a RNA:DNA hybrid. Our results suggest that, although crenarchaea and euryarchaea differ in chromosomal packaging, they share similar mechanisms in modulating strand displacement by DNA polymerases during lagging strand DNA synthesis.
机译:Euryarchaeota和Crenarchaeota是古细菌领域的两个主要谱系,它们编码不同的染色质蛋白,并且复制DNA聚合酶的用途也不同。 Crenarchaea拥有一个B族DNA聚合酶(PolB),能够通过染色质蛋白Cren7和Sul7d调节链位移。 Euryarchaea具有两种不同的复制性DNA聚合酶,即PolB和PolD,D家族DNA聚合酶。在这里,我们表征了来自嗜热性嗜热球菌激烈热球菌的PolB和PolD的链置换活性,并研究了狂热狂热真核生物组蛋白HPfA1对这些活动的影响。我们表明,PolB和PolD在链置换中均有效。 HPfA1抑制了两种DNA聚合酶的DNA链置换,但对退火成单链模板DNA的RNA链的置换几乎没有影响。这与发现HPfA1与双链DNA的结合比与RNA:DNA杂种的结合更紧密的发现是一致的。我们的结果表明,尽管crenarchaea和euryarchaea在染色体包装方面有所不同,但它们在滞后链DNA合成过程中在调节DNA聚合酶的链置换中具有相似的机制。

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