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 IIIit 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.

译文

通过遗传手段研究了大肠杆菌染色体上串联重复序列的重组机制。将624bp长的串联重复序列引入到大肠杆菌的lacZ基因中,并比较了不同重组突变体中一个重复序列的缺失效率。未检测到recA,recBC,recF,ruvA或ruvA recG突变的影响。因此,串联重复删除似乎不会通过RecBCD或RecF同源重组途径进行。分离出一个新的突变体,其中不依赖RecA的重组增加了15倍。该突变位于编码聚合酶IIIit的α亚基的dnaE基因,它是第133位密码子由Gly变为Asp的另一种dnaE突变,即dnaE486,经过测试,也显示出可刺激与RecA无关的重组。建议通过复制滑动机制发生串联-重复重组。不依赖RecA的重组在rep突变体中也得到增强,其中由于Rep解旋酶的缺乏而减慢了染色体的复制,这表明复制暂停可能有助于滑动。

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