The alleviation of DNA restriction during the SOS response in Escherichia coli has been further investigated. With the EcoK DNA restriction system UV irradiated wild-type cells show a 10(4)-fold increase in ability to plate non-modified lambda phage and a 3-4 fold increase in transformation by non-modified plasmid DNA. A role for the umuDC genes of E coli in the process of SOS-induced restriction alleviation was identified by showing that a umuC122::Tn5 mutant could alleviate EcoK restriction to only 5% that of wild-type levels. Although umuDC are better characterized for their pivotal role in SOS induced mutagenesis, it is demonstrated here that umu-dependent alleviation of EcoK restriction is a transient process in which umu-dependent mutagenesis plays little part. A second form of SOS induced alleviation of DNA restriction is described in this paper involving the McrA restriction system. The mcrA gene is shown to be encoded within a defective prophage called e14 situated at the 25 min region on the Escherichia coli genetic map. e14 is known to abortively excise from the chromosome after SOS induction and it is demonstrated in this report that mcrA is lost from the genome after SOS induction as part of e14. This results in co-ordinate decrease in the level of McrA restriction within a population of cells.

译文

:进一步研究了在大肠杆菌中SOS反应过程中DNA限制的减轻。使用EcoK DNA限制系统,紫外线照射的野生型细胞显示出接种未修饰的λ噬菌体的能力提高了10(4)倍,而未修饰的质粒DNA的转化率则提高了3-4倍。通过显示umuC122 :: Tn5突变体可以将EcoK限制降低到野生型水平的5%,从而确定了大肠杆菌的umuDC基因在SOS诱导的限制减轻过程中的作用。尽管umuDC因其在SOS诱变中的关键作用而得到了更好的表征,但在此证明了umu依赖性对EcoK限制的缓解是一个瞬态过程,其中umu依赖性诱变起着很小的作用。本文介绍了SOS诱导减轻DNA限制的第二种形式,涉及McrA限制系统。已显示mcrA基因被编码在大肠杆菌遗传图谱中位于25分钟区域的称为e14的缺陷前噬菌体中。已知e14在SOS诱导后从染色体上流产地切除,并且在本报告中证明,作为e14的一部分,在SOS诱导后mcrA从基因组中丢失。这导致细胞群中Mcrr限制水平的坐标降低。

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