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Role of RNA Decay in Bacterial Gene Regulation

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Microbiology".

Deadline for manuscript submissions: 31 May 2024 | Viewed by 613

Special Issue Editors


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Guest Editor
Academia Sinica, Institute of Molecular Biology, Taipei, Taiwan
Interests: RNA decay

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Guest Editor
Department of Immunology, Microbiology and Parasitology, Faculty of Science and Technology, University of the Basque Country, Barrio Sarriena, S/N, 48940 Leioa, Spain
Interests: bacterial stress responses; post-transcriptional control; small regulatory RNAs; RNA processing and decay; Escherichia coli; ecology of Vibrio species
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Special Issue Information

Dear Colleagues,

The marked ability of microorganisms to rapidly adapt to changing environments is largely rooted in their capacity to promptly reprogram gene expression by synthesizing new coding mRNAs, along with the concomitant elimination of redundant transcripts. The rapid and selective elimination of redundant bacterial transcripts is conducted by diverse mRNA decay machineries, the main components of which have been well characterized for a few model organisms including Escherichia coli and Bacillus subtilis. Various studies of mRNA decay mechanisms have shown that the 5′ phosphorylation status, nucleotide composition, and structure of individual mRNAs can greatly impact mRNA turnover, and they have revealed a number of cis-acting regulatory elements located within the 5′- and 3′ end regions. Some important cis-acting elements include 5′ stabilizers, riboswitches, repetitive extragenic palindromic sequences, and 3′ poly(A) tails, which regulate the accessibility of individual transcripts (or their segments) to different ribonucleases and regulatory factors. In addition to cis-acting elements, a number of trans-acting factors (e.g., small regulatory RNAs (sRNAs) and ribosomes) are likewise known for their essential roles in controlling RNA turnover under numerous stress conditions.

The major aim of this Special Issue is to draw attention to recent progress in the field, and, more specifically, to update the reader about (i) new RNA degradation mechanisms; (ii) the role of cis- and trans-acting mRNA stability determinants; and (iii) the multifaceted characteristics of RNA decay machineries, such as their diverse composition, biological functions, mechanisms of action, and phylogenetic conservation. Accordingly, we wish to invite prospective authors to submit original research and review articles focused on fundamental and applied aspects of RNA turnover in bacteria.

Potential topics include, but are not limited to, the following:

  • Advanced experimental approaches for monitoring the abundance and fate of RNA molecules.
  • Regulation of mRNA stability by cis-acting elements (RNA stabilizers, riboswitches, and polyadenylation).
  • Control of mRNA stability by small regulatory RNAs.
  • Interdependence of translation and mRNA decay.
  • Ribonucleases involved in RNA turnover and their ancillary factors.

Dr. Sue Lin-Chao
Prof. Dr. Vladimir Kaberdin
Guest Editors

Manuscript Submission Information

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

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Keywords

  • RNA stabilizers
  • RNA decay
  • RNA turnover
  • small regulatory RNAs
  • post-transcriptional control

Published Papers (1 paper)

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Research

23 pages, 2063 KiB  
Article
Hfq-Antisense RNA I Binding Regulates RNase E-Dependent RNA Stability and ColE1 Plasmid Copy Number
by Wei-Syuan Wang and Sue Lin-Chao
Int. J. Mol. Sci. 2024, 25(7), 3955; https://doi.org/10.3390/ijms25073955 - 02 Apr 2024
Viewed by 477
Abstract
The mechanisms and consequences of gene regulation by Hfq on trans-encoded small RNAs (sRNAs) have been well studied and documented. Recent employment of Genomic SELEX to search for Hfq-binding motifs has indicated that Hfq might frequently regulate gene expression controlled by cis [...] Read more.
The mechanisms and consequences of gene regulation by Hfq on trans-encoded small RNAs (sRNAs) have been well studied and documented. Recent employment of Genomic SELEX to search for Hfq-binding motifs has indicated that Hfq might frequently regulate gene expression controlled by cis-antisense RNAs. Here, we use the classic ColE1 plasmid antisense RNA-based regulation model (i.e., RNA I) to study the role of Hfq in controlling antisense regulatory functions. We show that Hfq exhibits a high binding affinity for RNA I and that binding limits RNase E cleavage, thereby stabilizing RNA I and reducing the plasmid copy number. Full-length RNA I displays a binding affinity for Hfq in the sub-micromolar range. In vivo overexpression of Hfq prolongs RNA I stability and reduces the ColE1 plasmid copy number, whereas deletion of hfq reduces RNA I stability and increases the plasmid copy number. RNA I predominantly binds to the proximal face of Hfq and exhibits competitive ability against a chromosome-borne proximal face-bound sRNA (DsrA) for Hfq binding. Through its strong promoter and high gene dosage features, plasmid-encoded antisense RNA I results in high RNA I expression, so it may antagonize the effects of trans-encoded RNAs in controlling target gene expression. Full article
(This article belongs to the Special Issue Role of RNA Decay in Bacterial Gene Regulation)
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