Holmberg C, Rutberg L
Department of Microbiology, University of Lund, Sweden.
Mol Microbiol. 1992 Oct;6(20):2931-8. doi: 10.1111/j.1365-2958.1992.tb01752.x.
The Bacillus subtilis glpD gene, encoding glycerol-3-phosphate (G3P) dehydrogenase, is preceded by a promoter and an inverted repeat which is located between the promoter and the glpD coding region. The inverted repeat acts as a transcriptional terminator in vitro. Expression of glpD is induced by G3P in the presence of the glpP gene product. Full-length glpD transcripts can be detected only in glycerol-induced cells. The major glpD transcript is initiated from the glpD promoter but minor amounts of larger transcripts, possibly initiated at upstream glp promoters, can also be found. In uninduced cells short transcripts are present, corresponding to initiation at the glpD promoter and termination at the inverted repeat. Upon induction, these short transcripts disappear and are replaced by full-length glpD transcripts. The 3'-ends of full-length glpD transcripts were mapped to an inverted repeat located immediately downstream of glpD. These results show that glpD of B. subtilis is regulated by termination/antitermination of transcription.
枯草芽孢杆菌的glpD基因编码甘油-3-磷酸(G3P)脱氢酶,其前面有一个启动子和一个反向重复序列,该反向重复序列位于启动子和glpD编码区之间。该反向重复序列在体外作为转录终止子起作用。在glpP基因产物存在的情况下,glpD的表达由G3P诱导。全长glpD转录本仅在甘油诱导的细胞中可检测到。主要的glpD转录本从glpD启动子起始,但也能发现少量可能从上游glp启动子起始的更大的转录本。在未诱导的细胞中存在短转录本,对应于从glpD启动子起始并在反向重复序列处终止。诱导后,这些短转录本消失,取而代之的是全长glpD转录本。全长glpD转录本的3'端被定位到紧邻glpD下游的一个反向重复序列。这些结果表明,枯草芽孢杆菌的glpD受转录终止/抗终止调控。