Small RNAs positively and negatively control transcription elongation through modulation of Rho utilization site accessibility

Bacteria use a multi-layered regulatory strategy to precisely and rapidly tune gene expression in response to environmental cues. Small RNAs (sRNAs) form an important layer of gene expression control and most act post-transcriptionally to control translation and stability of mRNAs. We have shown that at least five different sRNAs (RydC, CpxQ, ArrS, GcvB, and OxyS) in <i>Escherichia coli</i> regulate the cyclopropane fatty acid synthase (<i>cfa</i>) mRNA. These sRNAs bind at different sites in the long 5' untranslated region (UTR) of <i>cfa</i> mRNA, and previous work suggested that they modulate RNase E-dependent mRNA turnover. Rho-dependent transcription termination in the <i>cfa</i> 5'' UTR was demonstrated, leading us to hypothesize that the sRNAs might also regulate <i>cfa</i> transcription elongation. In this study, we find that a pyrimidine-rich region flanked by sRNA binding sites in the <i>cfa</i> 5' UTR is required for premature Rho-dependent termination. We discovered that sRNA-dependent regulation of <i>cfa</i> depends on Rho, and the activating sRNA RydC has only a minor effect on RNase E-mediated turnover of <i>cfa</i> mRNA. A stem-loop structure in the <i>cfa</i> 5' UTR sequesters the pyrimidine-rich region required for Rho-dependent termination. The repressing sRNA CpxQ binds to the 5' portion of the stem and increases Rho-dependent termination, whereas the activating sRNA RydC binds downstream of the stem and decreases termination. These results reveal the versatile mechanisms sRNAs use to regulate target gene expression at transcriptional and post-transcriptional levels and demonstrate that regulation by sRNAs in long UTRs can involve modulation of transcription elongation.IMPORTANCEBacteria respond to stress by rapidly regulating gene expression. Regulation can occur through the control of messenger RNA (mRNA) production (transcription elongation), stability of mRNAs, or translation of mRNAs. Bacteria can use small RNAs (sRNAs) to regulate gene expression at each of these steps, but we often do not understand how this works at a molecular level. In this study, we find that sRNAs in <i>Escherichia coli</i> regulate gene expression at the level of transcription elongation by promoting or inhibiting transcription termination by a protein called Rho. These results help us understand new molecular mechanisms of gene expression regulation in bacteria.

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Journal
mBio
Published
2025-10-31
DOI
https://doi.org/10.1128/mbio.02921-25
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
Field-Weighted Citation Impact
0.00
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article

Small RNAs positively and negatively control transcription elongation through modulation of Rho utilization site accessibility

Carin K. Vanderpool, Colleen Bianco, Kristen R. Farley, Andrew K. Buechler
mBio
Bacterial Genetics and Biotechnology
article

Small RNAs positively and negatively control transcription elongation through modulation of Rho utilization site accessibility

Carin K. Vanderpool, Colleen Bianco, Kristen R. Farley, Andrew K. Buechler
article en

Abstract

Bacteria use a multi-layered regulatory strategy to precisely and rapidly tune gene expression in response to environmental cues. Small RNAs (sRNAs) form an important layer of gene expression control and most act post-transcriptionally to control translation and stability of mRNAs. We have shown that at least five different sRNAs (RydC, CpxQ, ArrS, GcvB, and OxyS) in <i>Escherichia coli</i> regulate the cyclopropane fatty acid synthase (<i>cfa</i>) mRNA. These sRNAs bind at different sites in the long 5' untranslated region (UTR) of <i>cfa</i> mRNA, and previous work suggested that they modulate RNase E-dependent mRNA turnover. Rho-dependent transcription termination in the <i>cfa</i> 5'' UTR was demonstrated, leading us to hypothesize that the sRNAs might also regulate <i>cfa</i> transcription elongation. In this study, we find that a pyrimidine-rich region flanked by sRNA binding sites in the <i>cfa</i> 5' UTR is required for premature Rho-dependent termination. We discovered that sRNA-dependent regulation of <i>cfa</i> depends on Rho, and the activating sRNA RydC has only a minor effect on RNase E-mediated turnover of <i>cfa</i> mRNA. A stem-loop structure in the <i>cfa</i> 5' UTR sequesters the pyrimidine-rich region required for Rho-dependent termination. The repressing sRNA CpxQ binds to the 5' portion of the stem and increases Rho-dependent termination, whereas the activating sRNA RydC binds downstream of the stem and decreases termination. These results reveal the versatile mechanisms sRNAs use to regulate target gene expression at transcriptional and post-transcriptional levels and demonstrate that regulation by sRNAs in long UTRs can involve modulation of transcription elongation.IMPORTANCEBacteria respond to stress by rapidly regulating gene expression. Regulation can occur through the control of messenger RNA (mRNA) production (transcription elongation), stability of mRNAs, or translation of mRNAs. Bacteria can use small RNAs (sRNAs) to regulate gene expression at each of these steps, but we often do not understand how this works at a molecular level. In this study, we find that sRNAs in <i>Escherichia coli</i> regulate gene expression at the level of transcription elongation by promoting or inhibiting transcription termination by a protein called Rho. These results help us understand new molecular mechanisms of gene expression regulation in bacteria.

mBioVol. 16(12)
University of Illinois Urbana-Champaign (US)
Openalex Percentile: Top 66%
Bacterial Genetics and Biotechnology
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