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PMID: 2677602 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Molecular genetic analysis of FNR-dependent promoters.

Molecular microbiology ·Vol. 3 ·No. 7 ·1989-07-00 ·Pages 869-78

Eiglmeier K, Honoré N, Iuchi S, Lin EC, Cole ST

Abstract

In enteric bacteria, the expression of many genes encoding various anaerobic electron transfer functions is controlled by FNR, the product of the autoregulated fnr gene. FNR is structurally and functionally homologous to CAP, the catabolite gene activator protein, and increased FNR production strongly stimulates transcription of its target genes. By analysis of RNA produced in vivo the promoters of four FNR-dependent genes were localized and shown to display a common arrangement. A 22bp dyad symmetry was found about 30 nucleotides upstream of the transcriptional startpoints and a similar sequence was shown to overlap the site of transcription initiation in the negatively controlled fnr gene. The consensus sequence for the half site recognized by FNR (AAA-TTGAT) is only slightly different from that of CAP (AA-TGTGA). Studies with two mutant frd promoters from Escherichia coli, displaying altered regulation and FNR response, provided additional evidence for recognition of this sequence by FNR.

MeSH Terms
Bacterial Proteins/genetics,metabolism Base Sequence Binding Sites Escherichia coli/genetics Escherichia coli Proteins Gene Expression Regulation Iron-Sulfur Proteins Molecular Sequence Data Mutation Promoter Regions, Genetic RNA, Messenger/genetics Transcription Factors/genetics Transcription, Genetic
Chemicals
Bacterial Proteins Escherichia coli Proteins FNR protein, E coli Iron-Sulfur Proteins RNA, Messenger Transcription Factors
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Eiglmeier K
Laboratoire de Génétique Moléculaire Bactérienne, Institut Pasteur, Paris, France.
Honoré N
Iuchi S
Lin E C
Cole S T
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1989-07-00
Pages
869-78
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIGMS NIH HHS · 5-R01-GM11983 · United States
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