Brosse Anaïs, Korobeinikova Anna, Gottesman Susan, Guillier Maude
CNRS UMR8261, Associated with University Paris Diderot, Sorbonne Paris Cité, Institut de Biologie Physico-Chimique, 75005 Paris, France.
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Nucleic Acids Res. 2016 Nov 16;44(20):9650-9666. doi: 10.1093/nar/gkw642. Epub 2016 Jul 20.
Two-component systems (TCS) and small regulatory RNAs (sRNAs) are both widespread regulators of gene expression in bacteria. TCS are in most cases transcriptional regulators. A large class of sRNAs act as post-transcriptional regulators of gene expression that modulate the translation and/or stability of target-mRNAs. Many connections have been recently unraveled between these two types of regulators, resulting in mixed regulatory circuits with poorly characterized properties. This study focuses on the negative feedback circuit that exists between the EnvZ-OmpR TCS and the OmrA/B sRNAs. We have shown that OmpR directly activates transcription from the omrA and omrB promoters, allowing production of OmrA/B sRNAs that target multiple mRNAs, including the ompR-envZ mRNA. This control of ompR-envZ by the Omr sRNAs does not affect the amount of phosphorylated OmpR, i.e. the presumably active form of the regulator. Accordingly, expression of robust OmpR targets, such as the ompC or ompF porin genes, is not affected by OmrA/B. However, we find that several OmpR targets, including OmrA/B themselves, are sensitive to changing total OmpR levels. As a result, OmrA/B limit their own synthesis. These findings unravel an additional layer of control in the expression of some OmpR targets and suggest the existence of differential regulation within the OmpR regulon.
双组分系统(TCS)和小调控RNA(sRNA)都是细菌中广泛存在的基因表达调控因子。在大多数情况下,双组分系统是转录调控因子。一大类小调控RNA作为基因表达的转录后调控因子,调节靶标mRNA的翻译和/或稳定性。最近,这两种调控因子之间的许多联系已被揭示,形成了特性 poorly characterized 的混合调控回路。本研究聚焦于EnvZ-OmpR双组分系统与OmrA/B小调控RNA之间存在的负反馈回路。我们已经表明,OmpR直接激活omrA和omrB启动子的转录,从而产生靶向多种mRNA(包括ompR-envZ mRNA)的OmrA/B小调控RNA。Omr小调控RNA对ompR-envZ的这种调控并不影响磷酸化OmpR的量,即调控因子的可能活性形式。因此,强大的OmpR靶标(如ompC或ompF孔蛋白基因)的表达不受OmrA/B的影响。然而,我们发现几个OmpR靶标,包括OmrA/B自身,对总OmpR水平的变化敏感。结果,OmrA/B限制了它们自身的合成。这些发现揭示了一些OmpR靶标表达中的另一层调控,并表明在OmpR调控子内存在差异调控。