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Loss‐of‐function mutations in yjbD result in ClpX‐ and ClpP‐independent competence development of Bacillus subtilis
Author(s) -
Nakano Michiko M.,
Hajarizadeh Farin,
Zhu Yi,
Zuber Peter
Publication year - 2001
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.2001.02639.x
Subject(s) - biology , mutant , complementation , genetics , gene , bacillus subtilis , phenotype , ectopic expression , mutation , missense mutation , microbiology and biotechnology , bacteria
Mutations in clpP and clpX have pleiotropic effects on growth and developmentally regulated gene expression in Bacillus subtilis . ClpP and ClpX are needed for expression of comK , encoding the competence transcription factor required for the expression of genes within the competence regulon. ClpP, in combination with the ATPase ClpC, degrades the inhibitor of ComK, MecA. Proteolysis of MecA is stimulated by a small protein, ComS, which interacts with MecA. Suppressor mutations ( cxs ) were isolated that bypass the requirement for clpX for comK expression. These were found also to overcome the defect in comK expression conferred by a clpP mutation. These mutations were identified as missense mutations (cxs‐5, ‐7 and ‐12) and a nonsense (UAG) codon substitution (cxs‐10) in the yjbD coding sequence in a locus linked to mecA . That a yjbD disruption confers the cxs phenotype, together with its complementation by an ectopically expressed copy of yjbD , indicated that the suppressor alleles bear recessive, loss‐of‐function mutations of yjbD . ClpP‐ and ClpX‐independent comK expression rendered by inactivation of yjbD was still medium‐dependent and required ComS. MecA levels in a clpP‐yjbD mutant were lower that those of clpP mutant cells and ComK protein concentration in the clpP mutant was restored to wild‐type levels by the yjbD mutation. Consequently, the yjbD mutation bypasses the defect in competence development conferred by clpP and clpX . YjbD protein is barely detectable in wild‐type cells, but is present in large amounts in the clpP mutant cells. The results suggest that the role of ClpP in competence development is to degrade YjbD protein so that ComS can productively interact with the MecA–ClpC–ComK complex. Alternatively, the result could suggest that YjbD has a negative effect on regulated proteolysis and that MecA is degraded independently of ClpP when YjbD is absent.