Improved RNA stability estimation through Bayesian modeling reveals most Salmonella transcripts have subminute
Laura Jenniches1, Charlotte Michaux2, Linda Popella2
1Helmholtz Institute for RNA-based Infection Research, Helmholtz Centre for Infection Research, Würzburg 97080, Germany.
Summary
Bacterial RNA decay is regulated by RNA-binding proteins (RBPs). This study reveals RBPs like ProQ and CspC/E are crucial for RNA stability and gene expression, especially during stress.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- RNA decay is vital for gene expression regulation, particularly under environmental stress.
- Bacterial RNA-binding proteins (RBPs) influence posttranscriptional regulation, but their global effect on RNA stability is not fully understood.
Purpose of the Study:
- To investigate the role of major RBPs, ProQ and CspC/E, in maintaining RNA stability in *Salmonella enterica*.
- To identify transcripts with altered decay rates in the presence and absence of these RBPs.
Main Methods:
- Utilized rifampicin-induced RNA sequencing (RIF-seq) over a time course.
- Developed a hierarchical Bayesian model to analyze differential RNA decay.
- Integrated RIF-seq data with cross-linking and immunoprecipitation followed by RNA sequencing (CLIP-seq).
Main Results:
- The median RNA half-life in *Salmonella* was found to be less than 1 minute, significantly shorter than previously estimated.
- Over 50% of the longest-lived transcripts are bound by at least one major RBP.
- Absence of ProQ or CspC/E led to differential decay in 30-40% of their respective target transcripts, with ProQ implicated in oxidative stress response.
Conclusions:
- RBPs play a significant role in shaping the bacterial transcriptome by regulating RNA stability.
- ProQ and CspC/E are key regulators of RNA decay, influencing gene expression and stress responses in bacteria.
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