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PMID: 16436420 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Inhibition of competence development in Streptococcus pneumoniae by increased basal-level expression of the ComDE two-component regulatory system.

Microbiology (Reading, England) ·Vol. 152 ·No. Pt 2 ·2006-02-00 ·Pages 323-331

Guiral S, Hénard V, Granadel C, Martin B, Claverys JP

Abstract

Natural competence for genetic transformation in Streptococcus pneumoniae is controlled by the ComCDE signal-transduction pathway. Together, ComD, a membrane histidine kinase, and ComE, its cognate response regulator, constitute a typical two-component regulatory system involved in sensing the comC-encoded competence-stimulating peptide (CSP). The comCDE operon is strongly upregulated when CSP reaches a critical threshold, probably to coordinate competence induction throughout the population. During a study of the early regulation of the comCDE operon, a mutation which resulted in increased beta-galactosidase production from a comC : : lacZ fusion was isolated. This mutation, which was characterized as a G-->T change in the transcription terminator of the tRNA(Arg) located immediately upstream of comCDE, is suggested to destabilize the terminator and to allow transcriptional readthrough of comCDE. Here, it is shown that, quite unexpectedly, the mutation confers reduced transformability. A series of experiments undertaken with the aim of understanding this surprising phenotype is described. Evidence is presented that increased basal-level expression of comDE impedes both spontaneous and CSP-induced competence in S. pneumoniae. There is a discussion of how an increased concentration of ComD and/or ComE could affect competence development.

MeSH Terms
Bacterial Proteins/biosynthesis,genetics Gene Expression Regulation, Bacterial Histidine Kinase Mutation Operon/genetics Protein Kinases/chemistry,genetics,physiology Streptococcus pneumoniae/genetics,metabolism Transformation, Bacterial
Chemicals
Bacterial Proteins Protein Kinases Histidine Kinase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Guiral Sébastien
Laboratoire de Microbiologie et Génétique Moléculaires, UMR 5100 CNRS-Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Hénard Vincent
Laboratoire de Microbiologie et Génétique Moléculaires, UMR 5100 CNRS-Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Granadel Chantal
Laboratoire de Microbiologie et Génétique Moléculaires, UMR 5100 CNRS-Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Martin Bernard
Laboratoire de Microbiologie et Génétique Moléculaires, UMR 5100 CNRS-Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Claverys Jean-Pierre
Laboratoire de Microbiologie et Génétique Moléculaires, UMR 5100 CNRS-Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Article Info
Journal
Microbiology (Reading, England)
Abbr.
Microbiology (Reading)
ISSN
1350-0872
Published
2006-02-00
Pages
323-331
Language
English
Region
England
NLM ID
9430468
Subset
IM
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