Lomovskaya O L, Kidwell J P, Matin A
Department of Microbiology and Immunology, Stanford University, California 94305-5402.
J Bacteriol. 1994 Jul;176(13):3928-35. doi: 10.1128/jb.176.13.3928-3935.1994.
A reverse genetics approach was used to clone a pex starvation gene that codes for an 18-kDa polypeptide, designated PexB. Single-copy pexB-lacZ operon fusions were constructed to study transcriptional regulation and the promoter region of this gene. The induction by carbon starvation or osmotic stress was transcriptional and controlled by sigma 38 but was independent of this sigma factor by the oxidative stress; presumably, it was sigma 70 mediated under the latter stress. During nitrogen starvation, the induction was controlled at the posttranscriptional level. The pexB upstream region contained 245 nucleotides within which sequences approximating the consensus for cyclic AMP receptor protein and integration host factor binding sites were discernible. Deletion of 164 bp of the upstream region, which included these consensus sequences, did not affect starvation-or osmotic stress-mediated induction of pexB but abolished its induction by oxidative stress. The same start site was used in transcription during carbon starvation, osmotic stress, or oxidative stress, suggesting that the pexB promoter can be recognized in vivo by both sigma 38 and sigma 70, depending, presumably, on the presence of appropriate transcriptional factors. The -10 and -35 regions of pexB resembled those of some but not all genes known to be controlled by sigma 38.
采用反向遗传学方法克隆了一个编码18 kDa多肽的pex饥饿基因,命名为PexB。构建了单拷贝的pexB - lacZ操纵子融合体,以研究该基因的转录调控和启动子区域。碳饥饿或渗透胁迫诱导是转录性的,由σ38控制,但氧化胁迫诱导与该σ因子无关;推测在后者胁迫下是由σ70介导的。在氮饥饿期间,诱导是在转录后水平控制的。pexB上游区域包含245个核苷酸,其中可识别出近似于环腺苷酸受体蛋白和整合宿主因子结合位点共有序列的序列。上游区域164 bp的缺失,包括这些共有序列,不影响饥饿或渗透胁迫介导的pexB诱导,但消除了其氧化胁迫诱导。在碳饥饿、渗透胁迫或氧化胁迫期间转录使用相同的起始位点,这表明pexB启动子在体内可能由σ38和σ70识别,这可能取决于适当转录因子的存在。pexB的 - 10和 - 35区域类似于一些但并非所有已知受σ38控制的基因的相应区域。