Ogino Hidetaka, Teramoto Haruhiko, Inui Masayuki, Yukawa Hideaki
Research Institute of Innovative Technology for the Earth (RITE), Kyoto, Japan.
Mol Microbiol. 2008 Feb;67(3):597-608. doi: 10.1111/j.1365-2958.2007.06069.x. Epub 2007 Dec 12.
DNA damage-induced SOS response elicits the induction of cell-division suppressor as well as DNA repair genes. In Gram-positive bacteria, cell-division suppressor genes, so far characterized from Bacillus subtilis (yneA) and Mycobacterium tuberculosis (rv2719c), share limited homology, but are both located in the vicinity of lexA on their respective genomes. Using this proximity to lexA, Corynebacterium glutamicum R divS (cgR1759) was identified as an SOS-inducible cell-division suppressor in this study. The amino acid sequence of DivS showed no homology to that of YneA and Rv2719c. divS expression was markedly induced by DNA-damaging mitomycin C treatment in wild-type cells, but not in its DeltarecA mutant cells, which are unable to induce the SOS response. Wild-type C. glutamicum R cells exposed to DNA-damaging mitomycin C exhibited elongated morphology that, using green fluorescent protein-FtsZ fusion protein, was attributed to defects in FtsZ ring assembly. Cells defective in FtsZ ring assembly were subsequently incapable of septum wall synthesis. In the presence of mitomycin C, divS mutant cells did not exhibit this elongated morphology, whereas cells overexpressing divS were elongated and abnormally branched.
DNA损伤诱导的SOS反应会引发细胞分裂抑制因子以及DNA修复基因的诱导。在革兰氏阳性菌中,目前已从枯草芽孢杆菌(yneA)和结核分枝杆菌(rv2719c)中鉴定出细胞分裂抑制因子基因,它们的同源性有限,但在各自基因组中都位于lexA附近。利用与lexA的这种邻近关系,本研究中谷氨酸棒杆菌R的divS(cgR1759)被鉴定为一种SOS诱导型细胞分裂抑制因子。DivS的氨基酸序列与YneA和Rv2719c的氨基酸序列无同源性。在野生型细胞中,DNA损伤性丝裂霉素C处理可显著诱导divS表达,但在无法诱导SOS反应的DeltarecA突变细胞中则不会。暴露于DNA损伤性丝裂霉素C的野生型谷氨酸棒杆菌R细胞呈现出细长形态,利用绿色荧光蛋白-FtsZ融合蛋白,这种形态归因于FtsZ环组装缺陷。FtsZ环组装有缺陷的细胞随后无法进行隔膜壁合成。在丝裂霉素C存在的情况下,divS突变细胞未呈现出这种细长形态,而过度表达divS的细胞则细长且异常分支。