Domain Francis, Houot Laetitia, Chauvat Franck, Cassier-Chauvat Corinne
Service de Biochimie et Génétique Moléculaire,91191 Gif sur Yvette Cedex, France.
Mol Microbiol. 2004 Jul;53(1):65-80. doi: 10.1111/j.1365-2958.2004.04100.x.
The cyanobacterial genes lexA, recA and ruvB were analysed in Synechocystis PCC6803, which is shown here to be more radiation resistant than the other unicellular model strain Synechococcus PCC7942. We found that cyanobacteria do not have an Escherichia coli-type SOS regulon. The Synechocystis lexA and recA promoters were found to be strong and UV insensitive, unlike the ruvB promoter, which is weak and UV-C inducible. Yet, lexA and recA are regulated by UV-C, but the control is negative and occurs at the post-transcriptional level. Two novel conserved elements were characterized in the lexA promoter: (i) an unusually long crucial box 5'-TAAAATTTTGTATCTTTT-3' (-64, -47); and (ii) a negatively acting motif 5'-TAT GAT-3' (-42, -37). These elements were not found in the recA promoter, which appeared to be unusually simple in harbouring only a single crucial element (i.e. the canonical -10 box). RuvB, operating in recombination-dependent cellular processes, was found to be dispensable to cell growth, whereas LexA and RecA appeared to be critical to cell viability. Using DNA microarrays, we have identified 57 genes with expression that is altered, at least twofold, in response to LexA depletion. None of these genes is predicted to operate in DNA metabolism, arguing against the involvement of LexA in the regulation of DNA repair. Instead, most of the LexA-responsive genes were known to be involved in carbon assimilation or controlled by carbon availability. Consistently, the growth of the LexA-depleted strain was found to be strongly dependent on the availability of inorganic carbon.
对集胞藻PCC6803中的蓝藻基因lexA、recA和ruvB进行了分析,结果表明该藻比另一种单细胞模式菌株聚球藻PCC7942更耐辐射。我们发现蓝藻没有大肠杆菌类型的SOS调节子。与ruvB启动子不同,集胞藻lexA和recA启动子很强且对紫外线不敏感,ruvB启动子较弱且受UV-C诱导。然而,lexA和recA受UV-C调节,但这种调节是负向的,且发生在转录后水平。在lexA启动子中鉴定出两个新的保守元件:(i) 一个异常长的关键框5'-TAAAATTTTGTATCTTTT-3'(-64,-47);(ii) 一个负向作用基序5'-TAT GAT-3'(-42,-37)。在recA启动子中未发现这些元件,recA启动子似乎异常简单,仅含有一个关键元件(即典型的-10框)。RuvB在依赖重组的细胞过程中起作用,发现其对细胞生长是可有可无的,而LexA和RecA似乎对细胞活力至关重要。使用DNA微阵列,我们鉴定出57个基因,其表达因LexA缺失而至少改变两倍。预计这些基因中没有一个在DNA代谢中起作用,这表明LexA不参与DNA修复的调节。相反,大多数LexA反应性基因已知参与碳同化或受碳可用性控制。一致的是,发现LexA缺失菌株的生长强烈依赖于无机碳的可用性。