Wanner B L, Chang B D
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.
J Bacteriol. 1987 Dec;169(12):5569-74. doi: 10.1128/jb.169.12.5569-5574.1987.
The phoB and phoR genes encode a transcription activator and a sensory protein of the phosphate regulon, respectively. It is shown here that they were transcribed as an operon in which the phoB gene was promoter proximal. Although an operon structure was suggested previously (K. Makino, H. Shinagawa, M. Amemura, and A. Nakata, J. Mol. Biol. 190:37-44 and 192:549-556, 1986), previous results showed only that phoR gene expression during phosphate limitation is dependent on the upstream phoB promoter. The phoR gene could still have had its own promoter for expression in the presence of phosphate. Two polar transposon-induced mutations are described which simultaneously abolished phoB and phoR gene function in cis; one mutation mapped in the phoB gene, and the other mapped upstream of the phoB gene. These results demonstrate an operon structure, in which phoR gene function required expression from the phoB promoter. Unexpectedly, an antisense pho omega Mu d1(lacZ) insertion within the promoter-proximal end of the phoB gene expressed the lacZ reporter gene, thus allowing for the possibility that the phoBR operon is regulated by an antisense RNA.
phoB基因和phoR基因分别编码磷酸调节子的转录激活因子和传感蛋白。本文表明,它们作为一个操纵子进行转录,其中phoB基因位于启动子近端。尽管之前有人提出存在操纵子结构(K. Makino、H. Shinagawa、M. Amemura和A. Nakata,《分子生物学杂志》190:37 - 44及192:549 - 556,1986年),但之前的结果仅表明在磷酸盐限制期间phoR基因的表达依赖于上游的phoB启动子。在磷酸盐存在的情况下,phoR基因仍可能有其自身的启动子用于表达。本文描述了两个极性转座子诱导的突变,它们同时顺式消除了phoB和phoR基因的功能;一个突变位于phoB基因中,另一个位于phoB基因上游。这些结果证明了一种操纵子结构,其中phoR基因的功能需要从phoB启动子进行表达。出乎意料的是,在phoB基因启动子近端末端内的反义pho omega Mu d1(lacZ)插入表达了lacZ报告基因,因此使得phoBR操纵子可能受反义RNA调控。