Global Hfq-mediated RNA interactome of nitrogen starved Escherichia coli uncovers a conserved post-transcriptional regulatory axis required for optimal growth recovery

Author:

McQuail Josh1ORCID,Matera Gianluca2,Gräfenhan Tom3,Bischler Thorsten3,Haberkant Per4,Stein Frank4,Vogel Jörg25ORCID,Wigneshweraraj Sivaramesh1ORCID

Affiliation:

1. Section of Molecular Microbiology and Centre for Bacterial Resistance Biology, Faculty of Medicine, Imperial College London , UK

2. Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI) , D- 97080 Würzburg, Germany

3. Core Unit Systems Medicine, University of Würzburg , D- 97080 Würzburg, Germany

4. Proteomics Core Facility, EMBL Heidelberg ,  D- 69117, Heidelberg , Germany

5. Institute for Molecular Infection Biology (IMIB), Faculty of Medicine, University of Würzburg , D-97080 Würzburg, Germany

Abstract

Abstract The RNA binding protein Hfq has a central role in the post-transcription control of gene expression in many bacteria. Numerous studies have mapped the transcriptome-wide Hfq-mediated RNA–RNA interactions in growing bacteria or bacteria that have entered short-term growth-arrest. To what extent post-transcriptional regulation underpins gene expression in growth-arrested bacteria remains unknown. Here, we used nitrogen (N) starvation as a model to study the Hfq-mediated RNA interactome as Escherichia coli enter, experience, and exit long-term growth arrest. We observe that the Hfq-mediated RNA interactome undergoes extensive changes during N starvation, with the conserved SdsR sRNA making the most interactions with different mRNA targets exclusively in long-term N-starved E. coli. Taking a proteomics approach, we reveal that in growth-arrested cells SdsR influences gene expression far beyond its direct mRNA targets. We demonstrate that the absence of SdsR significantly compromises the ability of the mutant bacteria to recover growth competitively from the long-term N-starved state and uncover a conserved post-transcriptional regulatory axis which underpins this process.

Funder

Biotechnology and Biological Sciences Research Council Research

Leverhulme Trust Research Project

Imperial College UKRI OA

Publisher

Oxford University Press (OUP)

Subject

Genetics

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