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PMID: 15049827 Published · ppublish English Journal Article

clpC and clpP1P2 gene expression in Corynebacterium glutamicum is controlled by a regulatory network involving the transcriptional regulators ClgR and HspR as well as the ECF sigma factor sigmaH.

Molecular microbiology ·Vol. 52 ·No. 1 ·2004-04-00 ·Pages 285-302

Engels S, Schweitzer JE, Ludwig C, Bott M, Schaffer S

Abstract

The ATP-dependent protease Clp plays important roles in the cell's protein quality control system and in the regulation of cellular processes. In Corynebacterium glutamicum, the levels of the proteolytic subunits ClpP1 and ClpP2 as well as of the corresponding mRNAs were drastically increased upon deletion of the clpC gene, coding for a Clp ATPase subunit. We identified a regulatory protein, designated ClgR, binding to a common palindromic sequence motif in front of clpP1P2 as well as of clpC. Deletion of clgR in the DeltaclpC background completely abolished the increased transcription of both operons, indicating that ClgR activates transcription of these genes. ClgR activity itself is probably controlled via ClpC-dependent regulation of its stability, as ClgR is only present in DeltaclpC and not in wild-type cells, whereas the levels of clgR mRNA are comparable in both strains. clpC, clpP1P2 and clgR expression is induced upon severe heat stress, however, independently of ClgR. Identification of the heat-responsive transcriptional start sites in front of these genes revealed the presence of sequence motifs typical for sigmaECF-dependent promoters. The ECF sigma factor sigmaH could be identified as being required for transcriptional activation of clpC, clpP1P2 and clgR in response to severe heat stress. A second heat-responsive but sigmaH-independent promoter in front of clgR could be identified that is subject to negative regulation by the transcriptional repressor HspR. Taken together, these results show that clpC and clpP1P2 expression in C. glutamicum is subject to complex regulation via both independent and hierarchically organized pathways, allowing for the integration of multiple environmental stimuli. Both the ClgR- and sigmaH-dependent regulation of clpC and clpP1P2 expression appears to be conserved in other actinomycetes.

MeSH Terms
Adenosine Triphosphatases/genetics,metabolism Amino Acid Sequence Bacterial Proteins/genetics,metabolism Base Sequence Corynebacterium/genetics,physiology Endopeptidase Clp Gene Deletion Gene Expression Regulation, Bacterial Genes, Bacterial Heat-Shock Proteins/genetics,metabolism Heat-Shock Response Molecular Sequence Data Operon Promoter Regions, Genetic RNA, Messenger/analysis Regulon Repressor Proteins/metabolism Sequence Alignment Sequence Homology, Amino Acid Serine Endopeptidases/genetics,metabolism Sigma Factor/metabolism Transcription Initiation Site Transcription, Genetic Transcriptional Activation
Chemicals
Bacterial Proteins ClpC protein, Bacteria Heat-Shock Proteins HspR protein, bacteria RNA, Messenger Repressor Proteins Sigma Factor Serine Endopeptidases Endopeptidase Clp Adenosine Triphosphatases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Engels Sabine
Institute of Biotechnology 1, Research Centre Jülich, D-52425 Jülich, Germany.
Schweitzer Jens-Eric
Ludwig Carsten
Bott Michael
Schaffer Steffen
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2004-04-00
Pages
285-302
Language
English
Region
England
NLM ID
8712028
Subset
IM
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