Bierne H, Vilette D, Ehrlich S D, Michel B
Laboratoire de Génétique Microbienne, Institut National de la Recherche Agronomique, Jouy en Josas, France.
Mol Microbiol. 1997 Jun;24(6):1225-34. doi: 10.1046/j.1365-2958.1997.4381795.x.
The mechanism of recombination of tandem repeats in the chromosome of Escherichia coli was investigated by genetic means. Tandem repeats 624 bp long were introduced into the lacZ gene of E. coli and the efficiency of deletion of one repeat was compared in different recombination mutants. No effects of the recA, recBC, recF, ruvA or ruvA recG mutations were detected. Hence, tandem repeat deletion appears to not proceed via the RecBCD or RecF homologous recombination pathways. A new mutant in which RecA-independent recombination is increased 15-fold was isolated. The mutation lies in the dnaE gene coding for the alpha subunit of polymerase III: it is a Gly to Asp change at codon 133. Another dnaE mutation, dnaE486, was tested and also shown to stimulate RecA-independent recombination. It is proposed that tandem-repeat recombination occurs by a replication slippage mechanism. RecA-independent recombination is also enhanced in a rep mutant, in which chromosomal replication is slowed down by the absence of the Rep helicase, suggesting that replication pausing may facilitate slippage.
通过遗传学方法研究了大肠杆菌染色体中串联重复序列的重组机制。将624 bp长的串联重复序列导入大肠杆菌的lacZ基因,并比较了不同重组突变体中一个重复序列缺失的效率。未检测到recA、recBC、recF、ruvA或ruvA recG突变的影响。因此,串联重复序列的缺失似乎不是通过RecBCD或RecF同源重组途径进行的。分离出了一个新的突变体,其中不依赖RecA的重组增加了15倍。该突变位于编码聚合酶IIIα亚基的dnaE基因中:它是密码子133处的甘氨酸到天冬氨酸的变化。对另一个dnaE突变体dnaE486进行了测试,结果也表明它能刺激不依赖RecA的重组。有人提出串联重复序列的重组是通过复制滑动机制发生的。在rep突变体中,由于缺少Rep解旋酶,染色体复制减慢,不依赖RecA的重组也增强了,这表明复制暂停可能促进滑动。