Unidade Multidisciplinar de Genômica, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
J Bacteriol. 2011 Dec;193(24):6929-38. doi: 10.1128/JB.06015-11. Epub 2011 Oct 7.
The control of Vibrio cholerae phoBR expression by PhoB involves its binding to Pho boxes at -35 (box 1), -60 (box 2), and -80 (box 3) from the putative phoB translation start site. These loci were located in the sense (box 1) and antisense (boxes 2 and 3) strands of the phoBR regulatory region, and PhoB binds to these individual boxes with distinct affinities. Fusions of sequences containing different combinations of these boxes upstream of the lacZ reporter in a plasmid demonstrated that only those carrying boxes 1, 2, and 3, or 1 alone, activated transcription under inorganic phosphate (P(i)) limitation. When a fragment, including only boxes 1 and 2, was fused to lacZ, expression was no longer induced by low P(i), suggesting a repressive role for PhoBbox2 (PhoB bound to box 2) over the transcriptional activity induced by PhoBbox1. The similarity between lacZ expression levels from promoter fragments containing the three boxes or box 1 alone showed that PhoBbox3 eliminated the repressive effect imposed by PhoBbox2 on phoBR transcription. Complementation assays with a phoBR-containing plasmid demonstrated that the 234-bp promoter fragment carrying the three boxes is absolutely required for operon expression in Vibrio cholerae ΔphoBR cells. This was observed under P(i) abundance, when phoBR was expressed at a basal level and, also in low P(i) conditions, when Pho regulon genes were fully expressed. Thus, under P(i) limitation, PhoB exerts dual regulatory functions by binding sequentially distinct Pho boxes to enable the fine-tuning and precise control of phoBR expression in V. cholerae cells.
调控霍乱弧菌 phoBR 表达的 PhoB 通过与 phoB 翻译起始位点的-35(框 1)、-60(框 2)和-80(框 3)处的 Pho 盒结合来实现。这些基因座位于 phoBR 调控区的正义(框 1)和反义(框 2 和 3)链上,PhoB 与这些单独的框结合具有不同的亲和力。在质粒中,将包含这些框的不同组合的序列融合到 lacZ 报告基因的上游,证明只有那些携带框 1、2 和 3 或仅携带框 1 的质粒,在无机磷酸盐(Pi)限制下激活转录。当仅包含框 1 和 2 的片段与 lacZ 融合时,表达不再受低 Pi 诱导,这表明 PhoBbox2(与框 2 结合的 PhoB)对由 PhoBbox1 诱导的转录活性具有抑制作用。含有三个框或仅框 1 的启动子片段的 lacZ 表达水平的相似性表明,PhoBbox3 消除了 PhoBbox2 对 phoBR 转录的抑制作用。用含有 phoBR 的质粒进行互补测定表明,携带三个框的 234bp 启动子片段是霍乱弧菌ΔphoBR 细胞中操纵子表达所必需的。这在 Pi 丰富时观察到,当 phoBR 以基础水平表达时,并且在低 Pi 条件下,当 Pho 调控基因完全表达时,也观察到了这种情况。因此,在 Pi 限制下,PhoB 通过顺序结合不同的 Pho 盒发挥双重调节功能,从而实现了霍乱弧菌细胞中 phoBR 表达的精细调节和精确控制。