Wang L F, Doi R H
J Bacteriol. 1987 Sep;169(9):4190-5. doi: 10.1128/jb.169.9.4190-4195.1987.
The first gene of the Bacillus subtilis RNA polymerase sigma 43 operon, P23, has a protein-coding capacity of 23,000 daltons. Sequence analysis revealed three potential translational initiation sites within the same reading frame, which could encode proteins of 23,000 (P23), 19,000 (P19), and 9,000 (P9) daltons, respectively. An internal promoter (P3), which is expressed only during the sporulation stage, is located between the second and the third translational start sites. By protein fusion to the Escherichia coli beta-galactosidase gene, we showed that all three translational initiation sites of the P23 gene are used in vivo in both E. coli and B. subtilis, and regulation for differential expression of the three proteins during the development of B. subtilis is coupled to the transcriptional promoter switching mechanism. The physiological function of these multiple gene products is unknown and is currently under investigation.
枯草芽孢杆菌RNA聚合酶σ43操纵子的第一个基因P23,其蛋白质编码能力为23,000道尔顿。序列分析显示在同一阅读框内有三个潜在的翻译起始位点,它们分别可编码23,000道尔顿(P23)、19,000道尔顿(P19)和9,000道尔顿(P9)的蛋白质。一个仅在芽孢形成阶段表达的内部启动子(P3)位于第二个和第三个翻译起始位点之间。通过与大肠杆菌β-半乳糖苷酶基因进行蛋白质融合,我们发现P23基因的所有三个翻译起始位点在大肠杆菌和枯草芽孢杆菌体内均被使用,并且在枯草芽孢杆菌发育过程中这三种蛋白质差异表达的调控与转录启动子切换机制相关联。这些多个基因产物的生理功能尚不清楚,目前正在研究中。