Abstract

Flagellin (Hag) is one of the most abundant proteins in Bacillus subtilis Here we show that each flagellar filament is assembled from ∼12,000 Hag monomers and that there is a cytoplasmic pool of Hag that is restricted to 5% of the total. Hag is thought to be restricted at the level of translation by a partner-switching mechanism involving FliW and the homodimeric RNA-binding protein CsrA (CsrAdimer). We further show that the mechanism of translation inhibition is hypersensitive due to a 1:1 ratio of Hag to FliW, a 1:1 inhibitory ratio of FliW to CsrAdimer, and a nearly 1:1 ratio of CsrAdimer to hag transcripts. Equimolarity of all components couples single-molecule detection of Hag export to compensatory translation and causes cytoplasmic Hag concentrations to oscillate around the level of FliW. We found that stoichiometry is ensured by genetic architecture, translational coupling, and the ability of CsrAdimer to restrict hag transcript accumulation. We further show that homeostasis prevents Hag hyperaccumulation that would otherwise cause severe defects in intracellular architecture, perhaps due to increased molecular crowding. We note that FliW-CsrA-mediated structural homeostasis has similarities to that seen with some toxin-antitoxin systems.IMPORTANCE The intracellular concentration of flagellar filament protein Hag is restricted by the Hag-FliW-CsrA system in B. subtilis Here we show that the Hag-FliW-CsrAdimer system functions at nearly 1:1:1 stoichiometry and that the system is both robust with respect to perturbation and hypersensitive to the Hag intracellular concentration. Moreover, restriction of cytoplasmic Hag levels is important for maintaining proper intracellular architecture, as artificial Hag hyperaccumulation led to generalized spatial defects and a high frequency of minicell production. The Hag-FliW-CsrA system is conserved in the deeper branches of bacterial phylogeny, and we note that the Hag-FliW-CsrA "homeostasis module" resembles a toxin-antitoxin system where, by analogy, CsrA is the "toxin," FliW is the "antitoxin," and Hag is the target.

Highlights

  • Flagellin (Hag) is one of the most abundant proteins in Bacillus subtilis

  • Each filament is assembled from monomers of the protein flagellin that are synthesized in the cytoplasm and secreted by a dedicated type III secretion system within the flagellar basal body [11,12,13,14]

  • The flagellar filament is assembled from subunits of the Hag flagellin protein

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Summary

Introduction

Flagellin (Hag) is one of the most abundant proteins in Bacillus subtilis. Here we show that each flagellar filament is assembled from ϳ12,000 Hag monomers and that there is a cytoplasmic pool of Hag that is restricted to 5% of the total. Hag is thought to be restricted at the level of translation by a partner-switching mechanism involving FliW and the homodimeric RNA-binding protein CsrA (CsrAdimer). IMPORTANCE The intracellular concentration of flagellar filament protein Hag is restricted by the Hag-FliW-CsrA system in B. subtilis. In Bacillus subtilis, the Hag flagellin protein autoinhibits its translation through a partner-switching mechanism centered on the proteins FliW and CsrA [7] (Fig. 1A). When filament assembly is complete, secretion is reduced and Hag levels are thought to rise in the cytoplasm, causing Hag to bind to FliW and release CsrAdimer, thereby restoring the ability of CsrA to repress hag translation [7]. Hag-FliW-CsrA constitutes a three-node negative-feedback loop predicted to homeostatically restrict Hag levels within a narrow range of concentrations in the cytoplasm [7, 28]. The homeostatic level of Hag relative to that of FliW-CsrAdimer and the biological function for Hag homeostasis are poorly understood

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