Toyonaga T, Matsushita O, Katayama S, Minami J, Okabe A
Department of Microbiology, Kagawa Medical School, Japan.
Microbiol Immunol. 1992;36(6):603-13. doi: 10.1111/j.1348-0421.1992.tb02060.x.
The phospholipase C (alpha-toxin) gene (plc) of Clostridium perfringens was cloned into pUC19 and the effects of the upstream regions on expression of the plc gene were examined in Escherichia coli JM109. When the 0.7-kb region just upstream of the putative -35 site of the gene was deleted, production of phospholipase C increased approximately 10-fold. Northern blot hybridization analysis of the plc transcript showed that the upstream region inhibited transcription from the plc promoter. Nucleotide sequencing of this upstream region revealed that there are three periodically repeated (dA)5-6 tracts between positions -66 and -40 of the plc gene. A fragment containing this sequence showed anomalously slow electrophoretic mobility at low temperature, indicating that the region immediately upstream of the plc promoter is a locus of sequence directed DNA-bending. Nested deletions of the upstream region were created from its 5' end by exonuclease III and the effects of deletions on the expression of the plc gene were examined. When the 77-bp fragment containing the two (dA)5-6 tracts were deleted, phospholipase C production increased markedly. These results indicate that the intrinsic DNA curvature upstream of the plc promoter is involved in the negative regulation of the plc gene transcription.
将产气荚膜梭菌的磷脂酶C(α毒素)基因(plc)克隆到pUC19中,并在大肠杆菌JM109中检测其上游区域对plc基因表达的影响。当该基因推定的-35位点上游0.7 kb区域被缺失时,磷脂酶C的产量增加了约10倍。对plc转录本的Northern印迹杂交分析表明,上游区域抑制了plc启动子的转录。对该上游区域的核苷酸测序显示,在plc基因的-66至-40位之间有三个周期性重复的(dA)5-6序列片段。包含该序列的片段在低温下显示出异常缓慢的电泳迁移率,表明plc启动子紧邻的上游区域是序列导向DNA弯曲的位点。通过核酸外切酶III从其5'端对上游区域进行嵌套缺失,并检测缺失对plc基因表达的影响。当包含两个(dA)5-6序列片段的77 bp片段被缺失时,磷脂酶C的产量显著增加。这些结果表明,plc启动子上游固有的DNA弯曲参与了plc基因转录的负调控。