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DNA polymerase switching: effects on spontaneous mutagenesis in Escherichia coli.

机译:DNA聚合酶转换:对大肠杆菌中自发诱变的影响。

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Escherichia coli possesses five known DNA polymerases (pols). Pol III holoenzyme is the cell's main replicase, while pol I is responsible for the maturation of Okazaki fragments and filling gaps generated during nucleotide excision repair. Pols II, IV and V are significantly upregulated as part of the cell's global SOS response to DNA damage and under these conditions, may alter the fidelity of DNA replication by potentially interfering with the ability of pols I and III to complete their cellular functions. To test this hypothesis, we determined the spectrum of rpoB mutations arising in an isogenic set of mutL strains differentially expressing the chromosomally encoded pols. Interestingly, mutagenic hot spots in rpoB were identified that are susceptible to the actions of pols I-V. For example, in a recA730 lexA(Def) mutL background most transversions were dependent upon pols IV and V. In contrast, transitions were largely dependent upon pol I and to a lesser extent, pol III. Furthermore, the extent ofpol I-dependent mutagenesis at one particular site was modulated by pols II and IV. Our observations suggest that there is considerable interplay among all five E. coli polymerases that either reduces or enhances the mutagenic load on the E. coli chromosome.
机译:大肠杆菌拥有五种已知的DNA聚合酶(pols)。 Pol III全酶是细胞的主要复制酶,而Pol I则负责Okazaki片段的成熟并填补核苷酸切除修复过程中产生的缺口。 Pols II,IV和V作为细胞对DNA损伤的整体SOS反应的一部分而显着上调,在这些条件下,可能会潜在地干扰pols I和III完成其细胞功能的能力,从而改变DNA复制的保真度。为了验证这一假设,我们确定了在同基因组的mutL菌株中差异表达染色体编码pol的rpoB突变的光谱。有趣的是,在rpoB中发现了易受pol I-V作用诱变的热点。例如,在recA730 lexA(Def)mutL背景中,大多数转换取决于pols IV和V。相反,转换很大程度上取决于pol I,而在较小程度上取决于pol III。此外,在一个特定位点的pol I依赖性诱变的程度由pols II和IV调节。我们的观察结果表明,所有五种大肠杆菌聚合酶之间都有相当大的相互作用,可以降低或增强大肠杆菌染色体上的致突变性。

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