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PMID: 1698125 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Transcriptional antitermination in the bgl operon of E. coli is modulated by a specific RNA binding protein.

Cell ·Vol. 62 ·No. 6 ·1990-09-21 ·Pages 1153-63

Houman F, Diaz-Torres MR, Wright A

Abstract

Regulation of bgl operon expression in E. coli occurs by a mechanism involving antitermination of transcription at two termination sites within the operon. The bglG gene product is absolutely required for this process. Here we provide evidence that BglG is an RNA binding protein that recognizes a specific sequence located just upstream of each of the terminators. The sequence was delimited using a series of specific oligonucleotide probes. Mutational analysis of this sequence indicates that the protein requires a specific RNA secondary structure for recognition. We propose that BglG prevents transcription termination by binding to nascent RNA and blocking formation of the terminator structure.

MeSH Terms
Bacterial Proteins/genetics,metabolism Base Composition Base Sequence Binding Sites Carrier Proteins/genetics,metabolism Escherichia coli/genetics,metabolism Genes, Regulator Genetic Vectors Molecular Sequence Data Nucleic Acid Conformation Oligonucleotide Probes Operon Plasmids Protein Sorting Signals/genetics RNA, Bacterial/genetics,metabolism RNA-Binding Proteins Terminator Regions, Genetic Transcription, Genetic
Chemicals
Bacterial Proteins Carrier Proteins Oligonucleotide Probes Protein Sorting Signals RNA, Bacterial RNA-Binding Proteins antiterminator proteins, Bacteria
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Houman F
Department of Molecular Biology and Microbiology, Tufts University Health Sciences Campus, Boston, Massachusetts 02111.
Diaz-Torres M R
Wright A
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1990-09-21
Pages
1153-63
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM 38035 · United States
Databases
GENBANK
M16487
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