Methodologies for bacterial ribonuclease characterization using RNA-seq

Author:

Broglia Laura12ORCID,Le Rhun Anaïs13,Charpentier Emmanuelle14ORCID

Affiliation:

1. Max Planck Unit for the Science of Pathogens , D-10117 Berlin , Germany

2. Center for Human Technologies, Istituto Italiano di Tecnologia , 16152 Genova , Italy

3. Univ. Bordeaux, CNRS, INSERM, ARNA, UMR 5320 , U1212, F-33000 Bordeaux , France

4. Institute for Biology, Humboldt University , D-10115 Berlin , Germany

Abstract

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.

Funder

Max Planck Society

German Research Foundation

EMBO

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology

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