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DNA replication fidelity in Escherichia coli: A multi-DNA polymerase affair

机译:大肠杆菌中的DNA复制保真度:多DNA聚合酶事件

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High accuracy (fidelity) of DNA replication is important for cells to preserve the genetic identity and to prevent the accumulation of deleterious mutations. The error rate during DNA replication is as low as 10 ~(-9) to 10 ~(-11) errors per base pair. How this low level is achieved is an issue of major interest. This review is concerned with the mechanisms underlying the fidelity of the chromosomal replication in the model system Escherichia coli by DNA polymerase III holoenzyme, with further emphasis on participation of the other, accessory DNA polymerases, of which E. coli contains four (Pols I, II, IV, and V). Detailed genetic analysis of mutation rates revealed that (1) Pol II has an important role as a back-up proofreader for Pol III, (2) Pols IV and V do not normally contribute significantly to replication fidelity, but can readily do so under conditions of elevated expression, (3) participation of Pols IV and V, in contrast to that of Pol II, is specific to the lagging strand, and (4) Pol I also makes a lagging-strand-specific fidelity contribution, limited, however, to the faithful filling of the Okazaki fragment gaps. The fidelity role of the Pol III τ subunit is also reviewed.
机译:DNA复制的高准确性(保真度)对于细胞保持遗传特性并防止有害突变的积累非常重要。 DNA复制期间每个碱基对的错误率低至10〜(-9)至10〜(-11)个错误。如何实现这种低水平是一个重大关注的问题。这篇评论与DNA聚合酶III全酶在模型系统大肠杆菌中保真染色体复制的机制有关,并进一步强调了其他辅助DNA聚合酶的参与,其中大肠杆菌包含4种(大分子I, II,IV和V)。对突变率的详细遗传分析表明,(1)Pol II作为Pol III的后备校对者具有重要作用,(2)Pol IV和V通常不会显着促进复制保真度,但在一定条件下可以很容易地做到这一点。 (3)Pols IV和V的参与与Pol II的参与不同,它对落后链具有特异性,并且(4)Pol I也对滞后链具有一定的保真度,但有一定的局限性,忠实地填补了冈崎片段的空白。 Pol IIIτ亚基的保真作用也进行了综述。

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