Finch P W, Chambers P, Emmerson P T
J Bacteriol. 1985 Nov;164(2):653-8. doi: 10.1128/jb.164.2.653-658.1985.
The recA+ lexA+-dependent induction of four Escherichia coli SOS proteins was readily observed by two-dimensional gel analysis. In addition to the 38-kilodalton (kDa) RecA protein, which was induced in the greatest amounts and was readily identified, three other proteins of 115, 62, and 12 kDa were seen. The 115-kDa protein is the product of the uvrA gene, which is required for nucleotide excision repair and has previously been shown to be induced in the SOS response. The 62-kDa protein, which was induced to high intracellular levels, is the product of recN, a gene required for recBC-independent recombination. The recA and recN genes were partially derepressed in a recBC sbcB genetic background, a phenomenon which might account for the recombination proficiency of such strains. The 12-kDa protein has yet to be identified.
通过二维凝胶分析很容易观察到四种大肠杆菌SOS蛋白的recA⁺ lexA⁺依赖性诱导。除了诱导量最大且易于鉴定的38千道尔顿(kDa)RecA蛋白外,还观察到另外三种分别为115、62和12 kDa的蛋白。115 kDa的蛋白是uvrA基因的产物,核苷酸切除修复需要该基因,并且先前已证明其在SOS反应中被诱导。62 kDa的蛋白在细胞内被诱导到高水平,它是recN基因的产物,recBC非依赖性重组需要该基因。recA和recN基因在recBC sbcB遗传背景中部分去阻遏,这种现象可能解释了此类菌株的重组能力。12 kDa的蛋白尚未被鉴定。