Ventura Marco, Fitzgerald Gerald F, van Sinderen Douwe
Department of Microbiology, National University of Ireland, Western Road, Cork, Ireland.
Appl Environ Microbiol. 2005 Oct;71(10):6282-91. doi: 10.1128/AEM.71.10.6282-6291.2005.
A homolog of the clpC ATPase gene was identified in the genome of Bifidobacterium breve UCC 2003. Since this gene is very well conserved among eubacteria, we employed a PCR-based approach using primers based on highly conserved regions of ClpC proteins in order to identify homologous genes in other bifidobacterial species. Analysis by slot blot, Northern blot, and primer extension experiments showed that transcription of clpC is induced in response to moderate heat shock regimes. Moreover, we identified in the genome sequence of B. breve UCC 2003 a gene, designated clgR, which is predicted to encode a transcriptional regulator involved in regulation of the bifidobacterial clpC gene. The role of this protein in the regulation of B. breve UCC 2003 clpC gene expression was investigated by performing gel retardation experiments. We show that a biologically active ClgR molecule requires one or more proteinaceous coactivators to assist in the specific binding of ClgR to the clpC promoter region.
在短双歧杆菌UCC 2003的基因组中鉴定出了clpC ATP酶基因的一个同源物。由于该基因在真细菌中高度保守,我们采用基于聚合酶链反应(PCR)的方法,利用基于ClpC蛋白高度保守区域设计的引物,来鉴定其他双歧杆菌物种中的同源基因。狭缝印迹、Northern印迹和引物延伸实验分析表明,clpC的转录在适度热休克条件下被诱导。此外,我们在短双歧杆菌UCC 2003的基因组序列中鉴定出一个名为clgR的基因,预计该基因编码一种参与双歧杆菌clpC基因调控的转录调节因子。通过进行凝胶阻滞实验研究了该蛋白在短双歧杆菌UCC 2003 clpC基因表达调控中的作用。我们发现,一个具有生物活性的ClgR分子需要一种或多种蛋白质辅激活因子来协助ClgR与clpC启动子区域的特异性结合。