Nakamoto Hitoshi, Suzuki Michiru, Kojima Kouji
Department of Biochemistry and Molecular Biology, Saitama University, Saitama 338-8570, Japan.
FEBS Lett. 2003 Aug 14;549(1-3):57-62. doi: 10.1016/s0014-5793(03)00768-3.
To determine if the CIRCE/HrcA system operates in cyanobacteria, we have inactivated the hrcA repressor gene in Synechocystis sp. PCC 6803 by gene targeting. In the hrcA mutant, the groESL1 operon and the groEL2 gene, both of which have the CIRCE operator in their upstream regions, were derepressed at 30 degrees C without affecting expression of other major heat-shock genes. However, expression of these groE genes in the mutant was not fully derepressed. Their transcription increased further upon heat shock, and was initiated from the same sites as those used under normal conditions. This suggests that their expression is regulated by at least two different mechanisms, a negative one controlled by HrcA and an unknown positive one. The heat-induced expression of clpB1 and htpG was greatly repressed by the absence of HrcA. The hrcA mutant which constitutively overexpressed GroEL displayed improved cellular thermotolerance and also reduced photobleaching of phycocyanin under heat stress conditions.
为了确定CIRCE/HrcA系统是否在蓝细菌中发挥作用,我们通过基因靶向技术使集胞藻属PCC 6803中的hrcA阻遏基因失活。在hrcA突变体中,groESL1操纵子和groEL2基因(二者上游区域均含有CIRCE操纵元件)在30℃时去阻遏,且不影响其他主要热休克基因的表达。然而,突变体中这些groE基因的表达并未完全去阻遏。热休克时它们的转录进一步增加,且起始位点与正常条件下相同。这表明它们的表达受至少两种不同机制调控,一种是由HrcA控制的负调控机制,另一种是未知的正调控机制。HrcA缺失会极大地抑制clpB1和htpG的热诱导表达。组成型过表达GroEL的hrcA突变体在热胁迫条件下表现出细胞耐热性提高,藻蓝蛋白的光漂白也减少。