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Journal Article

Methodologies for bacterial ribonuclease characterization using RNA-seq.

MPS-Authors

Broglia,  Laura
Max Planck Unit for the Science of Pathogens, Max Planck Society;

Le Rhun,  Anaïs
Max Planck Unit for the Science of Pathogens, Max Planck Society;

Charpentier,  Emmanuelle
Max Planck Unit for the Science of Pathogens, Max Planck Society;

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Citation

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.


Cite as: https://hdl.handle.net/21.11116/0000-000D-CA22-9
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.