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PMID: 6447872 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Promoter for the establishment of repressor synthesis in bacteriophage lambda.

Schmeissner U, Court D, Shimatake H, Rosenberg M

Abstract

Transcription of the lambda repressor gene (cI) is positively regulated by the phage-encoded proteins cII and cIII. We have isolated and characterized the 5'-terminal region of this RNA and shown that it originates at a promoter (pE) located between genes cro and cII. The DNA sequence of this promoter shows little homology to other known promoters. Initiation of transcription from PE is abolished by the cis-dominant mutations cY; these mutations alter the "-10" and "-35" regions of the promoter. We propose that the "-35" region is the site of activation of PE, possibly via the direct interaction of protein cII.

MeSH Terms
Bacteriophage lambda/genetics Base Sequence Binding Sites Chromosome Mapping Cloning, Molecular Escherichia coli/genetics Genes, Regulator Mutation Operon Plasmids RNA Polymerase I/metabolism RNA, Messenger/isolation & purification Repressor Proteins/biosynthesis,genetics Transcription Factors/genetics Transcription, Genetic
Chemicals
RNA, Messenger Repressor Proteins Transcription Factors RNA Polymerase I
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schmeissner U
Court D
Shimatake H
Rosenberg M
References (37)
37 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1980-06-00
Pages
3191-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC349580
Subset
IM
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