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Identification of the epsilon-subunit of Escherichia coli DNA polymerase III holoenzyme as the dnaQ gene product: a fidelity subunit for DNA replication.

机译:鉴定大肠杆菌DNA聚合酶III全酶的ε亚基作为dnaQ基因产物:DNA复制的保真亚基。

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摘要

Based on extensive genetic and biochemical studies, the multisubunit DNA polymerase III holoenzyme is considered responsible for the chain-elongation stage in replication of the genome of Escherichia coli and is thus expected to be the major determinant of fidelity as well. Previous experiments have shown that two mutations conferring a very high mutation rate on E. coli, mutD5 and dnaQ49, decrease severely the 3' leads to 5' exonucleolytic editing activity of the polymerase III holoenzyme. To identify more precisely the nature of these mutations, we have carried out genetic mapping and complementation experiments. From these studies and experiments by others, we conclude that the most potent general mutator mutations in E. coli occur in a single gene, dnaQ. To define further the role of the dnaQ gene, we have used two-dimensional gel electrophoresis to compare the labeled dnaQ gene product with purified polymerase III holoenzyme. The dnaQ product comigrates with the epsilon-subunit, a 25-kilodalton protein of the polymerase III "core" enzyme. We conclude that the epsilon-subunit of polymerase III holoenzyme has a special role in defining the accuracy of DNA replication, probably through control of the 3' leads to 5' exonuclease activity.
机译:基于广泛的遗传和生化研究,多亚基DNA聚合酶III全酶被认为是大肠杆菌基因组复制过程中的链延长阶段,因此也有望成为保真度的主要决定因素。先前的实验表明,赋予大肠杆菌很高的突变率的两个突变mutD5和dnaQ49,严重降低了3'导致聚合酶III全酶的5'核酸外切编辑活性。为了更准确地确定这些突变的性质,我们进行了基因定位和互补实验。从其他人的这些研究和实验中,我们得出结论,大肠杆菌中最有效的一般突变体突变发生在单个基因dnaQ中。为了进一步定义dnaQ基因的作用,我们使用了二维凝胶电泳来比较标记的dnaQ基因产物与纯化的聚合酶III全酶。 dnaQ产物与ε-亚基(聚合酶III“核心”酶的25-千达尔顿蛋白)结合。我们得出结论,聚合酶III全酶的epsilon亚基在定义DNA复制的准确性中具有特殊作用,可能是通过控制3'导致5'核酸外切酶的活性。

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