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PMID: 8091212 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Synergistic activation of transcription by bacteriophage lambda cI protein and E. coli cAMP receptor protein.

Science (New York, N.Y.) ·Vol. 265 ·No. 5180 ·1994-09-23 ·Pages 1863-6

Joung JK, Koepp DM, Hochschild A

Abstract

Two heterologous prokaryotic activators, the bacteriophage lambda cI protein (lambda cI) and the Escherichia coli cyclic AMP receptor protein (CRP), were shown to activate transcription synergistically from an artificial promoter bearing binding sites for both proteins. The synergy depends on a functional activation (positive control) surface on each activator. These results imply that both proteins interact directly with RNA polymerase and thus suggest a precise mechanism for transcriptional synergy: the interaction of two activators with two distinct surfaces of RNA polymerase.

MeSH Terms
Base Sequence Binding Sites Cyclic AMP Receptor Protein/metabolism DNA-Binding Proteins DNA-Directed RNA Polymerases/metabolism Escherichia coli/enzymology,genetics Molecular Sequence Data Promoter Regions, Genetic Repressor Proteins/metabolism Transcription Factors/metabolism Transcriptional Activation Viral Proteins/metabolism Viral Regulatory and Accessory Proteins
Chemicals
Cyclic AMP Receptor Protein DNA-Binding Proteins Repressor Proteins Transcription Factors Viral Proteins Viral Regulatory and Accessory Proteins phage repressor proteins DNA-Directed RNA Polymerases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Joung J K
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA 02115.
Koepp D M
Hochschild A
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1994-09-23
Pages
1863-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIH HHS · DP1 OD006862 · United States
NIGMS NIH HHS · GM44025 · United States
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