Curti Elena, McDonald John P, Mead Samantha, Woodgate Roger
Laboratory of Genomic Integrity, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-3371, USA.
Mol Microbiol. 2009 Jan;71(2):315-31. doi: 10.1111/j.1365-2958.2008.06526.x. Epub 2008 Nov 4.
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 of pol 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.
大肠杆菌拥有五种已知的DNA聚合酶(Pol)。Pol III全酶是细胞的主要复制酶,而Pol I负责冈崎片段的成熟以及填补核苷酸切除修复过程中产生的缺口。作为细胞对DNA损伤的全局SOS反应的一部分,Pol II、IV和V显著上调,在这些条件下,它们可能通过潜在干扰Pol I和III完成其细胞功能的能力来改变DNA复制的保真度。为了验证这一假设,我们确定了在差异表达染色体编码的Pol的同基因mutL菌株组中出现的rpoB突变谱。有趣的是,在rpoB中发现了对Pol I-V的作用敏感的诱变热点。例如,在recA730 lexA(Def) mutL背景下,大多数颠换依赖于Pol IV和V。相比之下,转换很大程度上依赖于Pol I,在较小程度上依赖于Pol III。此外,Pol II和IV调节了一个特定位点上Pol I依赖性诱变的程度。我们的观察结果表明,所有五种大肠杆菌聚合酶之间存在相当大的相互作用,这种相互作用要么减少要么增加大肠杆菌染色体上的诱变负荷。