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Published on: March 15, 2011
ClpC and MecA, components of a proteolytic machine, prevent Spo0A-P-dependent transcription without degradation
Andrew W Tanner1, Valerie J Carabetta1,2, David Dubnau1,2
1Public Health Research Institute Center, New Jersey Medical School Rutgers University, Newark, NJ 07103, USA.
Abstract:
In Bacillus subtilis, a proteolytic machine composed of MecA, ClpC and ClpP degrades the transcription factor ComK, controlling its accumulation during growth. MecA also inhibits sporulation and biofilm formation by down-regulating spoIIG and sinI, genes that are dependent for their transcription on the phosphorylated protein Spo0A-P. Additionally, MecA has been shown to interact in vitro with Spo0A. Although the inhibitory effect on transcription requires MecA's binding partner ClpC, inhibition is not accompanied by the degradation of Spo0A, pointing to a previously unsuspected regulatory mechanism involving these proteins. Here, we further investigate the MecA and ClpC effects on Spo0A-P-dependent transcription. We show that MecA inhibits the transcription of several Spo0A-P activated genes, but fails to de-repress several Spo0A-P repressed promoters. This demonstrates that MecA and ClpC do not act by preventing the binding of Spo0A-P to its target promoters. Consistent with this, MecA by itself has no effect in vitro on the transcription from PspoIIG while the addition of both MecA and ClpC has a strong inhibitory effect. A complex of MecA and ClpC likely binds to Spo0A-P on its target promoters, preventing the activation of transcription. Thus, components of a degradative machine have been harnessed to directly repress transcription.
Insights
Bacillus subtilis uses MecA and ClpC proteins to directly repress transcription of Spo0A-P activated genes. This regulatory mechanism prevents gene activation without degrading the Spo0A-P transcription factor.
Area of Science:
- Microbiology
- Molecular Biology
- Gene Regulation
Background:
- Bacillus subtilis utilizes a proteolytic system involving MecA, ClpC, and ClpP to degrade the ComK transcription factor.
- MecA also inhibits sporulation and biofilm formation by down-regulating spoIIG and sinI, genes regulated by Spo0A-P.
- MecA interacts with Spo0A, suggesting a regulatory role beyond protein degradation.
Purpose of the Study:
- To investigate the regulatory mechanism of MecA and ClpC on Spo0A-P-dependent transcription.
- To determine how MecA and ClpC inhibit transcription without degrading Spo0A-P.
Main Methods:
- In vitro transcription assays using purified proteins and DNA templates.
- Analysis of MecA and ClpC effects on the transcription of Spo0A-P activated and repressed promoters.
Main Results:
- MecA and ClpC inhibit transcription of Spo0A-P activated genes but do not affect Spo0A-P repressed promoters.
- MecA alone does not inhibit transcription, but MecA and ClpC together strongly inhibit transcription from PspoIIG.
- MecA and ClpC do not prevent Spo0A-P binding to target promoters.
Conclusions:
- MecA and ClpC form a complex that directly represses transcription by binding to Spo0A-P on target promoters.
- This represents a novel regulatory mechanism where a proteolytic machine's components are repurposed for direct transcriptional repression.
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