Ahn K S, Malo M S, Smith M T, Wake R G
Department of Biochemistry, University of Sydney, NSW, Australia.
Gene. 1993 Sep 30;132(1):7-13. doi: 10.1016/0378-1119(93)90508-z.
One of two putative sigma A promoters identified previously in the region immediately upstream from the rtp gene (encoding the replication terminator protein) [Smith and Wake, J. Bacteriol. 170 (1988) 4083-4090] has been shown by transcription start point (tsp) mapping to be the functional rtp promoter. In these tsp mapping experiments, it was observed that the level of mRNA from this promoter, Prtp, was increased by a factor of 30 in the absence of the replication terminator protein (RTP), consistent with the autoregulation of rtp at the level of transcription. In vitro transcription from Prtp by sigma A RNA polymerase has been shown to be specifically repressed by RTP. A Prtp-spoVG-lacZ fusion was inserted into the chromosome of a strain in which RTP production was inducible by IPTG. Addition of IPTG to cultures of the new strain lowered beta Gal production by a factor of at least four. It is concluded that rtp is autoregulated in vivo at the level of transcription.
先前在rtp基因(编码复制终止蛋白)上游紧邻区域鉴定出的两个假定的σA启动子之一,经转录起始点(tsp)定位已表明是功能性的rtp启动子。在这些tsp定位实验中,观察到在没有复制终止蛋白(RTP)的情况下,来自该启动子Prtp的mRNA水平增加了30倍,这与rtp在转录水平的自动调节一致。已表明σA RNA聚合酶对Prtp的体外转录受到RTP的特异性抑制。将Prtp-spoVG-lacZ融合体插入到RTP产生可被IPTG诱导的菌株染色体中。向新菌株培养物中添加IPTG使β-半乳糖苷酶产量降低了至少四倍。得出的结论是,rtp在体内转录水平上受到自动调节。