Dynamic interactions between the RNA chaperone Hfq, small regulatory RNAs, and mRNAs in live bacterial cells

Author:

Park Seongjin1ORCID,Prévost Karine2,Heideman Emily M1,Carrier Marie-Claude2ORCID,Azam Muhammad S1,Reyer Matthew A3,Liu Wei1,Massé Eric2ORCID,Fei Jingyi13ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States

2. RNA Group, Department of Biochemistry, University of Sherbrooke, Sherbrooke, Canada

3. Institute for Biophysical Dynamics, The University of Chicago, Chicago, United States

Abstract

RNA-binding proteins play myriad roles in regulating RNAs and RNA-mediated functions. In bacteria, the RNA chaperone Hfq is an important post-transcriptional gene regulator. Using live-cell super-resolution imaging, we can distinguish Hfq binding to different sizes of cellular RNAs. We demonstrate that under normal growth conditions, Hfq exhibits widespread mRNA-binding activity, with the distal face of Hfq contributing mostly to the mRNA binding in vivo. In addition, sRNAs can either co-occupy Hfq with the mRNA as a ternary complex, or displace the mRNA from Hfq in a binding face-dependent manner, suggesting mechanisms through which sRNAs rapidly access Hfq to induce sRNA-mediated gene regulation. Finally, our data suggest that binding of Hfq to certain mRNAs through its distal face can recruit RNase E to promote turnover of these mRNAs in a sRNA-independent manner, and such regulatory function of Hfq can be decoyed by sRNA competitors that bind strongly at the distal face.

Funder

National Institutes of Health

Searle Scholars Program

Canadian Institutes of Health Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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