Abstract
Eo-E RNA polymerase transcribes a regulon of folding factors for the bacterial envelope and is induced by physical and chemical stresses. The RseA anti-sigma factor inhibits the activity of Esigma(E) RNA, polymerase. It is shown here that the N-terminal portion of sigma(E), residues 1-153, binds core RNA polymerase. RseA interacts with residues 154-191 of sigma(E), a site that is homologous to region 4, the sigma factor binding site for promoter DNA. Mutations that reduce transcription of Esigma(E) RNA polymerase map to sigma(E) residues 178, 181, and 183. Variant sigma(E) proteins with amino acid substitutions at residues 178, 181, or 183 do not associate with RseA. A regulatory mechanism is proposed whereby RseA binds to a C-terminal peptide of a-E and inhibits the transcription of Esigma(E) RNA polymerase by blocking promoter recognition.
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- Publication version
- Accepted or Published Version
- DOI:
- Digital Object Identifier (open in new tab) 10.1074/jbc.M202881200
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- Category:
- Articles
- Type:
- artykuły w czasopismach
- Published in:
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JOURNAL OF BIOLOGICAL CHEMISTRY
no. 277,
pages 27282 - 27287,
ISSN: 0021-9258 - Language:
- English
- Publication year:
- 2002
- Bibliographic description:
- Tam C., Collinet B., Lau G., Raina S., Missiakas D.: Interaction of the conserved region 4.2 of sigma(E) with the RseA anti-sigma factor// JOURNAL OF BIOLOGICAL CHEMISTRY -Vol. 277,iss. 30 (2002), s.27282-27287
- DOI:
- Digital Object Identifier (open in new tab) 10.1074/jbc.m202881200
- Verified by:
- Gdańsk University of Technology
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