DevA, a GntR-like transcriptional regulator required for development in streptomyces coelicolor

Tools

Hoskisson, Paul A. and Rigali, Sebastien and Fowler, Kay and Findlay, Kim C. and Buttner, Mark J. (2006) DevA, a GntR-like transcriptional regulator required for development in streptomyces coelicolor. Journal of Bacteriology, 188 (14). pp. 5014-5023. ISSN 1098-5530 (https://doi.org/10.1128/JB.00307-06)

[thumbnail of 314056.pdf]
Preview
 PDF. Filename: 314056.pdf
Accepted Author Manuscript
Download (1MB)| Preview

Abstract

The gram-positive filamentous bacterium Streptomyces coelicolor has a complex developmental cycle with three distinct phases: growth of the substrate mycelium, development of reproductive structures called aerial hyphae, and differentiation of these aerial filaments into long chains of exospores. During a transposon mutagenesis screen, we identified a novel gene (devA) required for proper development. The devA mutant produced only rare aerial hyphae, and those that were produced developed aberrant spore chains that were much shorter than wild-type chains and had misplaced septa. devA encodes a member of the GntR superfamily, a class of transcriptional regulators that typically respond to metabolite effector molecules. devA forms an operon with the downstream gene devB, which encodes a putative hydrolase that is also required for aerial mycelium formation on R5 medium. S1 nuclease protection analysis showed that transcription from the single devA promoter was temporally associated with vegetative growth, and enhanced green fluorescent protein transcriptional fusions showed that transcription was spatially confined to the substrate hyphae in the wild type. In contrast, devAB transcript levels were dramatically upregulated in a devA mutant and the devA promoter was also active in aerial hyphae and spores in this background, suggesting that DevA might negatively regulate its own production. This suggestion was confirmed by gel mobility shift assays that showed that DevA binds its own promoter region in vitro.

ORCID iDs

Hoskisson, Paul A. ORCID logoORCID: https://orcid.org/0000-0003-4332-1640, Rigali, Sebastien, Fowler, Kay, Findlay, Kim C. and Buttner, Mark J.;
CORE (COnnecting REpositories)