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Published on: February 23, 2021
Direct Inhibition of RetS Synthesis by RsmA Contributes to Homeostasis of the Pseudomonas aeruginosa Gac/Rsm
Jodi M Corley1, Peter Intile1, Timothy L Yahr1
1Department of Microbiology and Immunology, University of Iowa, Iowa City, Iowa, USAgrid.214572.7.
Abstract:
The Gac/Rsm system is a global regulator of Pseudomonas aeruginosa gene expression. The primary effectors are RsmA and RsmF. Both are RNA-binding proteins that interact with target mRNAs to modulate protein synthesis. RsmA/RsmF recognize GGA sequences presented in the loop portion of stem-loop structures. For repressed targets, the GGA sites usually overlap the ribosome binding site (RBS) and RsmA/RsmF binding inhibits translation initiation. RsmA/RsmF activity is controlled by several small non-coding RNAs (sRNA) that sequester RsmA/RsmF from target mRNAs. The most important sequestering sRNAs are RsmY and RsmZ. Transcription of rsmY/rsmZ is directly controlled by the GacSA two-component regulatory system. GacSA activity is antagonized by RetS, a hybrid sensor kinase. In the absence of retS, rsmY/rsmZ transcription is derepressed and RsmA/RsmF are sequestered by RsmY/RsmZ. Gac/Rsm system homeostasis is tightly controlled by at least two mechanisms. First, direct binding of RsmA to the rsmA and rsmF mRNAs inhibits further synthesis of both proteins. Second, RsmA stimulates rsmY/rsmZ transcription through an undefined mechanism. In this study we demonstrate that RsmA stimulates rsmY/rsmZ transcription by directly inhibiting RetS synthesis. RetS protein levels are elevated 2.5-fold in an rsmA mutant. Epistasis experiments demonstrate that the rsmA requirement for rsmY/rsmZ transcription is entirely suppressed in an rsmA, retS double mutant. RsmA directly interacts with the retS mRNA and requires two distinct GGA sites, one of which overlaps the RBS. We propose a model wherein RsmA inhibits RetS synthesis to promote rsmY/rsmZ transcription and that this acts as a checkpoint to limit RsmA/RsmF availability. IMPORTANCE The Pseudomonas aeruginosa Gac/Rsm system controls ∼500 genes and governs a critical lifestyle switch by inversely regulating factors that favor acute or chronic colonization. Control of gene expression by the Gac/Rsm system is mediated through RsmA and RsmF, small RNA-binding proteins that interact with target mRNAs to inhibit or promote protein synthesis and/or mRNA stability. RsmA/RsmF activity is governed by two small non-coding RNAs (RsmY and RsmZ) that sequester RsmA/RsmF from target mRNAs. The GacSA two-component regulatory system plays a pivotal role in the Gac/Rsm system by controlling rsmYZ transcription. This study provides insight into the control of homeostasis by demonstrating that RsmA directly targets and inhibits expression of RetS, an orphan sensor kinase critical for rsmYZ transcription.
Insights
The Pseudomonas aeruginosa Gac/Rsm system regulates gene expression. RsmA directly inhibits RetS synthesis, promoting rsmY/rsmZ transcription and controlling RsmA/RsmF availability for bacterial adaptation.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Gene Regulation
Background:
- The Gac/Rsm system in Pseudomonas aeruginosa globally regulates gene expression, impacting bacterial lifestyle.
- RsmA and RsmF are key RNA-binding proteins controlling protein synthesis by interacting with target mRNAs.
- RsmA/RsmF activity is modulated by small regulatory RNAs (RsmY/RsmZ) and the GacSA two-component system.
Purpose of the Study:
- To elucidate the mechanism by which RsmA stimulates rsmY/rsmZ transcription.
- To investigate the role of RetS in the Gac/Rsm regulatory network.
- To understand the homeostatic control of the Gac/Rsm system in Pseudomonas aeruginosa.
Main Methods:
- Epistasis experiments to define genetic interactions.
- Analysis of RetS protein levels in wild-type and mutant strains.
- RNA-binding assays to confirm RsmA interaction with retS mRNA.
Main Results:
- RsmA directly inhibits RetS synthesis by binding to the retS mRNA, overlapping the ribosome binding site.
- RetS protein levels were significantly elevated in an rsmA mutant.
- The requirement for rsmA in rsmY/rsmZ transcription was abolished in an rsmA, retS double mutant.
Conclusions:
- RsmA inhibits RetS production, which in turn promotes rsmY/rsmZ transcription.
- This mechanism acts as a checkpoint to regulate RsmA/RsmF availability and maintain Gac/Rsm system homeostasis.
- The findings provide new insights into the complex regulatory network governing Pseudomonas aeruginosa gene expression and adaptation.
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