Home LiteratureArticle Details
PMID: 1703923 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A consensus motif common to all Rho-dependent prokaryotic transcription terminators.

Cell ·Vol. 64 ·No. 3 ·1991-02-08 ·Pages 553-63

Alifano P, Rivellini F, Limauro D, Bruni CB, Carlomagno MS

Abstract

We have characterized at the molecular level several polar mutations in four different cistrons of the his operon of S. typhimurium. An analysis of the his-specific transcripts produced in vivo in the mutant strains, together with in vitro transcription assays, led to the identification of several cryptic Rho-dependent transcription termination elements within the his operon that are activated by the uncoupling of transcription and translation. Common features of these elements were sought and found with a computer program. We have identified a consensus motif, consisting of a cytosine-rich and guanosine-poor region, that is located upstream of the heterogeneous 3' endpoints of the prematurely terminated in vivo transcripts and that is present in all the Rho-dependent transcription terminators described thus far.

Related Genes
MeSH Terms
Base Sequence Blotting, Northern Cloning, Molecular DNA, Bacterial/genetics Histidine Molecular Sequence Data Mutation Operon RNA, Bacterial/genetics RNA, Messenger/genetics Regulatory Sequences, Nucleic Acid Restriction Mapping Rho Factor/physiology Salmonella typhimurium/genetics Terminator Regions, Genetic Transcription, Genetic
Chemicals
DNA, Bacterial RNA, Bacterial RNA, Messenger Rho Factor Histidine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Alifano P
Dipartimento di Biologia e Patologia Cellulare e Molecolare, Università di Napoli, Italy.
Rivellini F
Limauro D
Bruni C B
Carlomagno M S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1991-02-08
Pages
553-63
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Databases
GENBANK
M58327, M58328, M58329, M59201, M94285, S63145, S63146, S63147, S63148, X13464
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