Elledge S J, Walker G C
J Mol Biol. 1983 Feb 25;164(2):175-92. doi: 10.1016/0022-2836(83)90074-8.
umuC is the genetic locus showing the greatest specificity for the "error-prone repair" process that is responsible for u.v. and chemical mutagenesis in Escherichia coli. By generating a probe specific to umuC DNA, we have been able to clone the umuC locus. Through a combination of subcloning and Tn1000 mutagenesis, we have identified a region of 2.2 X 10(3) bases which contains the information necessary to complement umuC mutations. This region of DNA codes for two polypeptides with molecular weights of 16,000 and 45,000. The genes for these proteins are organized in an operon that is repressed by the lexA protein. Complementation of previously isolated umuC mutations revealed that these proteins correspond to two complementation groups, umuC, which codes for the 45,000 Mr protein, and umuD, which codes for the 16,000 Mr protein, and that therefore both proteins are essential for "error-prone repair" in E. coli.
umuC是对“易错修复”过程具有最大特异性的基因位点,该过程负责大肠杆菌中的紫外线和化学诱变。通过生成特异于umuC DNA的探针,我们得以克隆umuC基因位点。通过亚克隆和Tn1000诱变相结合,我们鉴定出一个2.2×10³个碱基的区域,该区域包含互补umuC突变所需的信息。这段DNA区域编码两种分子量分别为16,000和45,000的多肽。这些蛋白质的基因组成一个操纵子,受lexA蛋白抑制。对先前分离的umuC突变进行互补分析表明,这些蛋白质对应于两个互补组,umuC编码45,000 Mr的蛋白质,umuD编码16,000 Mr的蛋白质,因此这两种蛋白质对大肠杆菌中的“易错修复”都是必不可少的。