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PMID: 3313282 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Competition between sigma factors for core RNA polymerase.

Nucleic acids research ·Vol. 15 ·No. 20 ·1987-10-26 ·Pages 8521-30

Malik S, Zalenskaya K, Goldfarb A

Abstract

The switch of RNA polymerase specificity from early to late promoters of bacteriophage T4 is achieved by substitution of host sigma factor, sigma 70, with the T4 induced factor, sigma gp55. However, overproduction of sigma gp55 from an expression vector is not detrimental to Escherichia coli growth. Direct competition binding assays demonstrate that sigma 70 readily displaces sigma gp55 from RNA polymerase and thereby reverses the promoter specificity of the enzyme. The displacement also occurs with the core enzyme modified by bacteriophage T4 infection. We postulate that an antagonist of sigma 70 should be formed in T4-infected cells to aid sigma gp55 in the early/late switch.

MeSH Terms
Binding, Competitive DNA-Directed RNA Polymerases/metabolism Escherichia coli/genetics,metabolism Kinetics Promoter Regions, Genetic Protein Binding Sigma Factor/genetics T-Phages/genetics,metabolism Transcription Factors/genetics Transcription, Genetic
Chemicals
Sigma Factor Transcription Factors DNA-Directed RNA Polymerases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Malik S
Department of Microbiology, Columbia University College of Physicians and Surgeons, New York, NY 10032.
Zalenskaya K
Goldfarb A
References (17)
17 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1987-10-26
Pages
8521-30
Language
English
Region
England
NLM ID
0411011
PMCID
PMC306375
Subset
IM
Grants
NIGMS NIH HHS · GM 30717 · United States
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