REGULATORY INPUTS FOR THE SYNTHESIS OF COMK, THE COMPETENCE TRANSCRIPTION FACTOR OF BACILLUS-SUBTILIS

Citation
J. Hahn et al., REGULATORY INPUTS FOR THE SYNTHESIS OF COMK, THE COMPETENCE TRANSCRIPTION FACTOR OF BACILLUS-SUBTILIS, Molecular microbiology, 21(4), 1996, pp. 763-775
Citations number
40
Categorie Soggetti
Biology,Microbiology
Journal title
ISSN journal
0950382X
Volume
21
Issue
4
Year of publication
1996
Pages
763 - 775
Database
ISI
SICI code
0950-382X(1996)21:4<763:RIFTSO>2.0.ZU;2-7
Abstract
Competence in Bacillus subtilis is expressed post-exponentially in res ponse to signals which are interpreted by a complex network of regulat ory proteins. This network culminates in the transcriptional activatio n of a set of late-competence proteins that mediate DNA binding and up take during transformation. ComK, a protein that binds to competence p romoters and appears to activate their transcription, is itself synthe sized in response to the signal-transduction network. ComK is known to be required for the transcription of its own gene. We have placed com K under control of the xylose-inducible PxylA promoter and used this c onstruct to show that ComK synthesis is sufficient as well as necessar y to induce competence. We have also confirmed that the Mec proteins a ct posttranscriptionally to inactivate ComK, probably by protein-prote in interaction. We have further demonstrated that ComS is required to generate an upstream signal that causes reversal of Mec-induced inacti vation of ComK. In addition to ComK itself, DegU, AbrB, and SinR are r equired for comK transcription; mutations in their genes are bypassed by PxylA-comK induction, and therefore their products appear not to ac t via the Mec proteins. Overproduction of ComK, in a loss-of-function mec mutant, is also known to bypass the need for DegU, SinR and AbrB. We propose that these proteins enhance the activity of ComK as a posit ive autoregulatory transcription factor, acting as coactivator protein s when ComK is present at low concentrations. Finally, we demonstrate that when ComK is synthesized from the PxylA promoter and mecA is inac tivated by mutation, no additional growth-stage-regulated control of c ompetence can be detected.