Belitsky Boris R, Brinsmade Shaun R, Sonenshein Abraham L
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, United States of America.
PLoS Genet. 2015 Oct 16;11(10):e1005600. doi: 10.1371/journal.pgen.1005600. eCollection 2015 Oct.
The global transcriptional regulator, CodY, binds strongly to the regulatory region of the braB gene, which encodes a Bacillus subtilis branched-chain amino acid (BCAA) permease. However, under conditions that maximize CodY activity, braB expression was similar in wild-type and codY null mutant cells. Nonetheless, expression from the braB promoter was significantly elevated in cells containing partially active mutant versions of CodY or in wild-type cells under growth conditions leading to intermediate levels of CodY activity. This novel pattern of regulation was shown to be due to two opposing mechanisms, negative and positive, by which CodY affects braB expression. A strong CodY-binding site located downstream of the transcription start point conferred negative regulation by direct interaction with CodY. Additionally, sequences upstream and downstream of the promoter were required for repression by a second pleiotropic B. subtilis regulator, ScoC, whose own expression is repressed by CodY. ScoC-mediated repression of braB in codY null mutants cells was as efficient as direct, CodY-mediated repression in wild-type cells under conditions of high CodY activity. However, under conditions of reduced CodY activity, CodY-mediated repression was relieved to a greater extent than ScoC-mediated repression was increased, leading to elevated braB expression. We conclude that restricting increased expression of braB to conditions of moderate nutrient limitation is the raison d'être of the feed-forward regulatory loop formed by CodY and ScoC at the braB promoter. The increase in BraB expression only at intermediate activities of CodY may facilitate the uptake of BCAA when they are not in excess but prevent unneeded BraB synthesis when other BCAA transporters are active.
全局转录调节因子CodY与braB基因的调控区域紧密结合,braB基因编码一种枯草芽孢杆菌的支链氨基酸(BCAA)通透酶。然而,在使CodY活性最大化的条件下,野生型和codY基因敲除突变体细胞中的braB表达相似。尽管如此,在含有部分活性突变型CodY的细胞中,或者在导致CodY活性处于中等水平的生长条件下的野生型细胞中,braB启动子的表达显著升高。这种新的调控模式被证明是由于CodY影响braB表达的两种相反机制,即负调控和正调控。位于转录起始点下游的一个强CodY结合位点通过与CodY直接相互作用赋予负调控。此外,启动子上下游的序列对于另一种枯草芽孢杆菌的多效调节因子ScoC的抑制作用是必需的,ScoC自身的表达受到CodY的抑制。在高CodY活性条件下,ScoC在codY基因敲除突变体细胞中介导的对braB的抑制作用与野生型细胞中CodY直接介导的抑制作用一样有效。然而,在CodY活性降低的条件下,CodY介导的抑制作用比ScoC介导的抑制作用解除的程度更大,导致braB表达升高。我们得出结论,将braB表达的增加限制在适度营养限制的条件下,是CodY和ScoC在braB启动子处形成的前馈调节环存在的理由。仅在CodY的中等活性时BraB表达增加,可能在BCAA不过量时促进其摄取,但在其他BCAA转运蛋白活跃时防止不必要的BraB合成。