Tapias A, Barbé J
Department of Genetics and Microbiology, Faculty of Sciences, Universitat Autònoma de Barcelona, Bellaterra, Spain.
Mol Gen Genet. 1999 Aug;262(1):121-30. doi: 10.1007/s004380051066.
The Sinorhizobium meliloti uvrA gene was isolated by complementation of a Rhodobacter sphaeroides UvrA- mutant. DNA sequencing of the region upstream of the S. meliloti uvrA gene reveals the presence of the ssb gene in the opposite transcriptional orientation. PCR-mediated mutagenesis demonstrated that expression of these two genes is inducible by DNA damage, and depends, in both cases, on the direct repeat GTTCN7GTTC (cited according to the direction of uvrA transcription). Comparison of the sequences of recA and uvrA promoters from different bacterial species of the alpha group of the Proteobacteria has identified the direct repeat GTTCYYKTTTTGTTC as the SOS box in this phylogenetic group.
通过对球形红杆菌UvrA突变体进行互补,分离出了苜蓿中华根瘤菌uvrA基因。苜蓿中华根瘤菌uvrA基因上游区域的DNA测序显示,存在转录方向相反的ssb基因。PCR介导的诱变表明,这两个基因的表达可由DNA损伤诱导,并且在这两种情况下,都依赖于直接重复序列GTTCN7GTTC(根据uvrA转录方向引用)。对变形菌门α亚群不同细菌物种的recA和uvrA启动子序列进行比较,确定直接重复序列GTTCYYKTTTTGTTC为本系统发育组中的SOS框。