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Transcription and translation of the sigG gene is tuned for proper execution of the switch from early to late gene expression in the developing Bacillus subtilis spore

A cascade of alternative sigma factors directs developmental gene expression during spore formation by the bacterium Bacillus subtilis. As the spore develops, a tightly regulated switch occurs in which the early-acting sigma factor σ(F) is replaced by the late-acting sigma factor σ(G). The gene enco...

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Detalles Bibliográficos
Autores principales: Mearls, Elizabeth B., Jackter, Jacquelin, Colquhoun, Jennifer M., Farmer, Veronica, Matthews, Allison J., Murphy, Laura S., Fenton, Colleen, Camp, Amy H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5942855/
https://www.ncbi.nlm.nih.gov/pubmed/29702640
http://dx.doi.org/10.1371/journal.pgen.1007350
Descripción
Sumario:A cascade of alternative sigma factors directs developmental gene expression during spore formation by the bacterium Bacillus subtilis. As the spore develops, a tightly regulated switch occurs in which the early-acting sigma factor σ(F) is replaced by the late-acting sigma factor σ(G). The gene encoding σ(G) (sigG) is transcribed by σ(F) and by σ(G) itself in an autoregulatory loop; yet σ(G) activity is not detected until σ(F)-dependent gene expression is complete. This separation in σ(F) and σ(G) activities has been suggested to be due at least in part to a poorly understood intercellular checkpoint pathway that delays sigG expression by σ(F). Here we report the results of a careful examination of sigG expression during sporulation. Unexpectedly, our findings argue against the existence of a regulatory mechanism to delay sigG transcription by σ(F) and instead support a model in which sigG is transcribed by σ(F) with normal timing, but at levels that are very low. This low-level expression of sigG is the consequence of several intrinsic features of the sigG regulatory and coding sequence—promoter spacing, secondary structure potential of the mRNA, and start codon identity—that dampen its transcription and translation. Especially notable is the presence of a conserved hairpin in the 5’ leader sequence of the sigG mRNA that occludes the ribosome-binding site, reducing translation by up to 4-fold. Finally, we demonstrate that misexpression of sigG from regulatory and coding sequences lacking these features triggers premature σ(G) activity in the forespore during sporulation, as well as inappropriate σ(G) activity during vegetative growth. Altogether, these data indicate that transcription and translation of the sigG gene is tuned to prevent vegetative expression of σ(G) and to ensure the precise timing of the switch from σ(F) to σ(G) in the developing spore.