Cell Biology and Metabolism Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.
Mol Microbiol. 2010 Mar;75(5):1215-31. doi: 10.1111/j.1365-2958.2010.07044.x. Epub 2010 Jan 12.
Small RNAs (sRNAs) that act by base pairing with trans-encoded mRNAs modulate metabolism in response to a variety of environmental stimuli. Here, we describe an Hfq-binding sRNA (FnrS) whose expression is induced upon a shift from aerobic to anaerobic conditions and which acts to downregulate the levels of a variety of mRNAs encoding metabolic enzymes. Anaerobic induction in minimal medium depends strongly on FNR but is also affected by the ArcA and CRP transcription regulators. Whole genome expression analysis showed that the levels of at least 32 mRNAs are downregulated upon FnrS overexpression, 15 of which are predicted to base pair with FnrS by TargetRNA. The sRNA is highly conserved across its entire length in numerous Enterobacteria, and mutational analysis revealed that two separate regions of FnrS base pair with different sets of target mRNAs. The majority of the target genes were previously reported to be downregulated in an FNR-dependent manner but lack recognizable FNR binding sites. We thus suggest that FnrS extends the FNR regulon and increases the efficiency of anaerobic metabolism by repressing the synthesis of enzymes that are not needed under these conditions.
小 RNA(sRNA)通过与反式编码的 mRNA 碱基配对来调节代谢,以响应各种环境刺激。在这里,我们描述了一种 Hfq 结合的 sRNA(FnrS),其表达在从需氧到厌氧条件的转变时被诱导,并且可以下调多种编码代谢酶的 mRNA 的水平。在最小培养基中的厌氧诱导强烈依赖于 FNR,但也受到 ArcA 和 CRP 转录调节剂的影响。全基因组表达分析表明,FnrS 过表达时至少有 32 个 mRNA 的水平下调,其中 15 个被预测通过 TargetRNA 与 FnrS 碱基配对。该 sRNA 在许多肠杆菌中全长高度保守,突变分析表明 FnrS 的两个不同区域与不同的靶 mRNA 对碱基配对。大多数靶基因以前被报道以 FNR 依赖的方式下调,但缺乏可识别的 FNR 结合位点。因此,我们认为 FnrS 通过抑制在这些条件下不需要的酶的合成来扩展 FNR 调控组,并提高厌氧代谢的效率。