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海拉细胞单链DNA结合蛋白在体外提高了DNA聚合酶α进行DNA合成的准确性。

HeLa cell single-stranded DNA-binding protein increases the accuracy of DNA synthesis by DNA polymerase alpha in vitro.

作者信息

Carty M P, Levine A S, Dixon K

机构信息

Section on Viruses and Cellular Biology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892.

出版信息

Mutat Res. 1992 Jun;274(1):29-43. doi: 10.1016/0921-8777(92)90041-z.

Abstract

To determine whether cellular replication factors can influence the fidelity of DNA replication, the effect of HeLa cell single-stranded DNA-binding protein (SSB) on the accuracy of DNA replication by HeLa cell DNA polymerase alpha has been examined. An in vitro gap-filling assay, in which the single-stranded gap contains the supF target gene, was used to measure mutagenesis. Addition of SSB to the in vitro DNA synthesis reaction increased the accuracy of DNA polymerase alpha by 2- to 8-fold. Analysis of the products of DNA synthesis indicated that SSB reduces pausing by the polymerase at specific sites in the single-stranded supF template. Sequence analysis of the types of errors resulting from synthesis in the absence or presence of SSB reveals that, while the errors are primarily base substitutions under both conditions, SSB reduces the number of errors found at 3 hotspots in the supF gene. Thus, a cellular replication factor (SSB) can influence the fidelity of a mammalian DNA polymerase in vitro, suggesting that the high accuracy of cellular DNA replication may be determined in part by the interaction between replication factors, DNA polymerase and the DNA template in the replication complex.

摘要

为了确定细胞复制因子是否会影响DNA复制的保真度,研究人员检测了HeLa细胞单链DNA结合蛋白(SSB)对HeLa细胞DNA聚合酶α进行DNA复制准确性的影响。采用体外填补缺口试验,其中单链缺口中含有supF靶基因,以此来测定诱变作用。在体外DNA合成反应中添加SSB,可使DNA聚合酶α的准确性提高2至8倍。对DNA合成产物的分析表明,SSB减少了聚合酶在单链supF模板上特定位点的停顿。对在不存在或存在SSB的情况下合成所产生的错误类型进行序列分析发现,虽然在两种条件下错误主要都是碱基替换,但SSB减少了在supF基因中3个热点处发现的错误数量。因此,一种细胞复制因子(SSB)在体外可影响哺乳动物DNA聚合酶的保真度,这表明细胞DNA复制的高准确性可能部分取决于复制因子、DNA聚合酶和复制复合物中DNA模板之间的相互作用。

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