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PMID: 8022288 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Rho and RNA: models for recognition and response.

Molecular microbiology ·Vol. 11 ·No. 6 ·1994-03-00 ·Pages 983-90

Platt T

Abstract

Escherichia coli Rho factor is required for termination of transcription at certain sites by RNA polymerase. Binding to unstructured cytosine-containing RNA target sites, subsequent RNA-dependent ATP hydrolysis, and an RNA-DNA helicase activity that presumably facilitates termination, are considered essential for Rho function. Yet the RNA recognition elements have remained elusive, the parameters relating RNA binding to ATPase activation have been obscure, and the mechanistic steps that integrate Rho's characteristics with its termination function in vitro and in vivo have been largely undefined. Recent work offers new insights into these interactions with results that are both surprising and satisfying in the context of Rho's emerging structure. These include the requirements for binding and ATPase activation by a variety of RNA substrates, dynamic analyses of Rho tracking, helicase and termination activity, and the participation of a new factor (NusG) that interacts with Rho. Models for Rho function are considered in the light of these recent revelations.

Related Genes
MeSH Terms
Bacterial Proteins/metabolism DNA-Directed RNA Polymerases/metabolism Escherichia coli/genetics Escherichia coli Proteins Models, Genetic Peptide Elongation Factors/metabolism Rho Factor/metabolism Terminator Regions, Genetic Transcription Factors Transcription, Genetic
Chemicals
Bacterial Proteins Escherichia coli Proteins NusG protein, E coli Peptide Elongation Factors Rho Factor Transcription Factors DNA-Directed RNA Polymerases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Platt T
Department of Biochemistry, University of Rochester Medical Center, New York 14642.
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1994-03-00
Pages
983-90
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIGMS NIH HHS · GM-2-R01-35658 · United States
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