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Open AccessJournal ArticleDOI

Comparative genomics provides structural and functional insights into Bacteroides RNA biology

TLDR
In this paper, a comparative genomics approach was used to investigate RNA biology in an understudied gut bacterium, using Bacteroides thetaiotaomicron as a representative microbiota member.
Abstract
Bacteria employ noncoding RNA molecules for a wide range of biological processes, including scaffolding large molecular complexes, catalyzing chemical reactions, defending against phages, and controlling gene expression. Secondary structures, binding partners, and molecular mechanisms have been determined for numerous small noncoding RNAs (sRNAs) in model aerobic bacteria. However, technical hurdles have largely prevented analogous analyses in the anaerobic gut microbiota. While experimental techniques are being developed to investigate the sRNAs of gut commensals, computational tools and comparative genomics can provide immediate functional insight. Here, using Bacteroides thetaiotaomicron as a representative microbiota member, we illustrate how comparative genomics improves our understanding of RNA biology in an understudied gut bacterium. We investigate putative RNA-binding proteins and predict a Bacteroides cold-shock protein homolog to have an RNA-related function. We apply an in silico protocol incorporating both sequence and structural analysis to determine the consensus structures and conservation of nine Bacteroides noncoding RNA families. Using structure probing, we validate and refine these predictions and deposit them in the Rfam database. Through synteny analyses, we illustrate how genomic coconservation can serve as a predictor of sRNA function. Altogether, this work showcases the power of RNA informatics for investigating the RNA biology of anaerobic microbiota members.

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Posted ContentDOI

An integrated transcriptomics–functional genomics approach reveals a small RNA that modulates Bacteroides thetaiotaomicron sensitivity to tetracyclines

TL;DR: In this paper , the authors map transcriptional units and profile their expression levels in Bacteroides thetaiotaomicron over a suite of 15 defined experimental conditions that are relevant in vivo, such as variation of temperature, pH, and oxygen tension, exposure to antibiotic stress, and growth on simple carbohydrates or on host mucin derived glycans.
References
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Journal ArticleDOI

Tunable Expression Tools Enable Single-Cell Strain Distinction in the Gut Microbiome

TL;DR: A platform for engineering Bacteroides, the most abundant genus in the Western microbiota, is described, which includes a process for high-throughput strain modification and a novel phage promoter and translational tuning strategy, and an unprecedented level of expression is achieved that enables imaging of fluorescent-protein-expressing Bactseroides stably colonizing the mouse gut.
Journal ArticleDOI

Suppression of a cold-sensitive mutation in 16S rRNA by overexpression of a novel ribosome-binding factor, RbfA.

TL;DR: The observed patterns of allele specificity of suppression and synthetic lethality in cells containing an RBFA knockout in combination with various 16S rRNA mutations suggests that RbfA interacts with the 5'-terminal helix region of 16SrRNA, possibly during a late step of 30S maturation.
Journal ArticleDOI

SRP-RNA sequence alignment and secondary structure

TL;DR: The secondary structures of the RNAs from the signal recognition particle, termed SRP-RNA, were derived buy comparative analyses of an alignment of 39 sequences and represent refinements of earlier versions and include a new short helix.
Journal ArticleDOI

Role of 4.5S RNA in Assembly of the Bacterial Signal Recognition Particle with Its Receptor

TL;DR: Surprisingly, 4.5S RNA facilitates both assembly and disassembly of the Ffh-FtsY complex to a similar extent, providing an example of an RNA molecule facilitating protein-protein interactions in a catalytic fashion.
Journal ArticleDOI

RNA remodeling and gene regulation by cold shock proteins.

TL;DR: One of the many important consequences that temperature down-shift has on cells is stabilization of secondary structures of RNAs, which has wide-spread effects, such as inhibition of expression of several genes due to termination of their transcription and inefficient RNA degradation that adversely affect cell growth at low temperature.
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