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  Methodologies for bacterial ribonuclease characterization using RNA-seq.

Broglia, L., Le Rhun, A., & Charpentier, E. (2023). Methodologies for bacterial ribonuclease characterization using RNA-seq. FEMS microbiology reviews, 47(5). doi:10.1093/femsre/fuad049.

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 Creators:
Broglia, Laura1, Author
Le Rhun, Anaïs1, Author
Charpentier, Emmanuelle1, Author
Affiliations:
1Max Planck Unit for the Science of Pathogens, Max Planck Society, ou_3213696              

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Free keywords: *Endoribonucleases, *Ribonucleases/genetics, Bacteria/genetics, post-transcriptional regulation, Ribonucleases, RNA, RNA decay, RNA degradation, RNA processing, RNA sequencing, RNA-Seq, transcriptomics
 Abstract: Bacteria adjust gene expression at the post-transcriptional level through an intricate network of small regulatory RNAs and RNA-binding proteins, including ribonucleases (RNases). RNases play an essential role in RNA metabolism, regulating RNA stability, decay, and activation. These enzymes exhibit species-specific effects on gene expression, bacterial physiology, and different strategies of target recognition. Recent advances in high-throughput RNA sequencing (RNA-seq) approaches have provided a better understanding of the roles and modes of action of bacterial RNases. Global studies aiming to identify direct targets of RNases have highlighted the diversity of RNase activity and RNA-based mechanisms of gene expression regulation. Here, we review recent RNA-seq approaches used to study bacterial RNases, with a focus on the methods for identifying direct RNase targets.

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 Dates: 2023-09
 Publication Status: Issued
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 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1093/femsre/fuad049
BibTex Citekey: broglia_methodologies_2023
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Title: FEMS microbiology reviews
Source Genre: Journal
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Pages: - Volume / Issue: 47 (5) Sequence Number: - Start / End Page: - Identifier: ISSN: 1574-6976 0168-6445