Takahashi Yukari, Yamaguchi Osamu, Omata Tatsuo
Laboratory of Molecular Plant Physiology, Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan.
Mol Microbiol. 2004 May;52(3):837-45. doi: 10.1111/j.1365-2958.2004.04021.x.
The cmp operon of Synechococcus sp. strain PCC 7942, encoding a high-affinity bicarbonate transporter, is induced under low CO(2) conditions by a LysR family protein CmpR. CmpR was found to be required also for induction of the operon by transfer of the cells from low-light to high-light conditions, indicating involvement of a common mechanism in the high-light- and low-CO(2)-responsive regulation. Expression of the high-light inducible genes psbAII and psbAIII, on the other hand, was found to be induced also by low-CO(2) conditions. A single promoter was responsible for the high-light and low-CO(2) induction of each of psbAII and psbAIII, suggesting involvement of a common regulatory mechanism in the light and CO(2) responses of the psbA genes. CmpR was, however, not required for the induction of psbAII and psbAIII, indicating the presence of multiple mechanisms for induction of genes under high-light and low-CO(2) conditions. The CmpR-deficient mutant nevertheless showed lower levels of the psbAII and psbAIII transcripts than the wild-type strain under all the light and CO(2) conditions examined. Gel shift assays showed that CmpR binds to the enhancer elements of psbAII and psbAIII, through specific interaction with a sequence signature conforming to the binding motif of similar LysR family proteins. These findings showed that CmpR acts as a trans-acting factor that enhances transcription of the photosystem II genes involved in acclimation to high light, revealing a complex network of gene regulation in the cyanobacterium.
聚球藻属PCC 7942菌株的cmp操纵子编码一种高亲和力碳酸氢盐转运蛋白,在低二氧化碳条件下由LysR家族蛋白CmpR诱导表达。研究发现,当细胞从低光照转移到高光照条件时,CmpR对于该操纵子的诱导也是必需的,这表明在高光和低二氧化碳响应调节中存在共同机制。另一方面,高光诱导基因psbAII和psbAIII的表达也被发现可由低二氧化碳条件诱导。一个单一的启动子负责psbAII和psbAIII各自的高光和低二氧化碳诱导,这表明在psbA基因的光照和二氧化碳响应中存在共同的调节机制。然而,psbAII和psbAIII的诱导不需要CmpR,这表明在高光和低二氧化碳条件下基因诱导存在多种机制。尽管如此,在所有检测的光照和二氧化碳条件下,CmpR缺陷型突变体的psbAII和psbAIII转录本水平均低于野生型菌株。凝胶迁移实验表明,CmpR通过与符合相似LysR家族蛋白结合基序的序列特征进行特异性相互作用,从而与psbAII和psbAIII的增强子元件结合。这些发现表明,CmpR作为一种反式作用因子,增强了参与适应高光的光系统II基因的转录,揭示了蓝细菌中复杂的基因调控网络。