Ouyang S, Sau S, Lee C Y
Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
J Bacteriol. 1999 Apr;181(8):2492-500. doi: 10.1128/JB.181.8.2492-2500.1999.
The production of type 8 capsular polysaccharide (CP8) in Staphylococcus aureus is regulated in response to a variety of environmental factors. The cap8 genes required for the CP8 production in strain Becker are transcribed as a single large transcript by a primary promoter located within a 0.45-kb region upstream of the first gene of the cap8 gene cluster. In this study, we analyzed the primary cap8 promoter region in detail. We determined the transcription initiation site of the primary transcript by primer extension and identified the potential promoter sequences. We found several inverted and direct repeats upstream of the promoter. Deletion analysis and site-directed mutagenesis showed that a 10-bp inverted repeat of one of the repeats was required for promoter activity. We showed that the distance but not the specific sequences between the inverted repeat and the promoter was critical to the promoter activity. However, insertion of a DNA sequence with two or four helix turns in this intervening region had a slight effect on promoter activity. To demonstrate the biological significance of the 10-bp inverted repeat, we constructed a strain with a mutation in the repeat in the S. aureus Becker chromosome and showed that the repeat affected CP8 production mostly at the transcriptional level. By gel mobility shift assay, we demonstrated that strain Becker produced at least one protein capable of specific binding to the 10-bp inverted repeat, indicating that the repeat serves as a positive regulatory protein binding site. In addition, reporter gene fusion analysis showed that the cap8 promoter activity was influenced by various growth media and affected most by yeast extract. Our results suggest that yeast extract may exert its profound inhibitory effect on cap8 gene expression through the 10-bp inverted repeat element.
金黄色葡萄球菌中8型荚膜多糖(CP8)的产生受多种环境因素调控。Becker菌株中CP8产生所需的cap8基因由位于cap8基因簇第一个基因上游0.45 kb区域内的一个主要启动子转录为一个单一的大转录本。在本研究中,我们详细分析了cap8主要启动子区域。我们通过引物延伸确定了主要转录本的转录起始位点,并鉴定了潜在的启动子序列。我们在启动子上游发现了几个反向和正向重复序列。缺失分析和定点诱变表明,其中一个重复序列的10 bp反向重复对于启动子活性是必需的。我们发现反向重复序列与启动子之间的距离而非特定序列对启动子活性至关重要。然而,在这个间隔区域插入具有两个或四个螺旋圈的DNA序列对启动子活性有轻微影响。为了证明10 bp反向重复序列的生物学意义,我们构建了一株在金黄色葡萄球菌Becker染色体上该重复序列发生突变的菌株,并表明该重复序列主要在转录水平上影响CP8的产生。通过凝胶迁移率变动分析,我们证明Becker菌株产生了至少一种能够特异性结合10 bp反向重复序列的蛋白质,表明该重复序列作为一个正向调节蛋白结合位点。此外,报告基因融合分析表明,cap8启动子活性受多种生长培养基影响,其中酵母提取物的影响最大。我们的结果表明,酵母提取物可能通过10 bp反向重复元件对cap8基因表达产生深远的抑制作用。