Document Detail


The finM promoter and the traM promoter are the principal promoters of the traM gene of the antibiotic resistance plasmid R100.
MedLine Citation:
PMID:  9402017     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
finP multicopy repression and traJ multicopy derepression indicate that the ratio of sense to antisense transcripts is important in the regulation of R100 conjugation. The extension of R100 traM transcripts into traJ shows that promoters in traM can affect this ratio, making the regulation of traM transcription important in the regulation of R100 conjugation. Since R100 traM, traY and tral proteins bind to the traM promoter region, we examined traM transcription in R100-1 traM, traY and tral mutants and compared it with traM transcription in both R100-1 and R100. We verified that the traM and finM promoters provide virtually all the transcripts originating in the R100-1 traM gene. When either is deleted, as in VAR22 or VAR30, the remaining promoter is highly active. We show here that traY positively regulates R100-1 traM transcription, as has been found for F. We found that tral did not regulate R100-1 traM transcription. The measured activity of the native R100 traM promoter was 12% of that in R100-1, whereas the native R100 finM promoter was 45% of that in R100-1. These data and data from the R100-1 traY and tral mutants show that the activities of the two promoters varied independently.
Authors:
D T Stockwell; W B Dempsey
Related Documents :
23640037 - Glucocorticoid induction of occludin expression and endothelial barrier requires transc...
1438227 - Regulation of balb/c 3t3 fibroblast proliferation by b-myb is accompanied by selective ...
18459127 - The functional -443t/c osteopontin promoter polymorphism influences osteopontin gene ex...
23147197 - Drugging the undruggable: transcription therapy for cancer.
18437897 - Regulation of programmed cell death by nf-kappab and its role in tumorigenesis and ther...
20135207 - Model analysis of the concentration-dependent permeability of p-gp substrates.
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Molecular microbiology     Volume:  26     ISSN:  0950-382X     ISO Abbreviation:  Mol. Microbiol.     Publication Date:  1997 Nov 
Date Detail:
Created Date:  1998-02-19     Completed Date:  1998-02-19     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  8712028     Medline TA:  Mol Microbiol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  455-67     Citation Subset:  IM    
Affiliation:
Veterans Affairs Medical Center, Dallas, TX 75216, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Bacterial Proteins / genetics*
Base Sequence
DNA Primers
DNA, Bacterial
Densitometry
Drug Resistance, Microbial / genetics*
Escherichia coli Proteins*
Molecular Sequence Data
Promoter Regions, Genetic*
R Factors / genetics*
RNA-Binding Proteins*
Repressor Proteins*
Ribonuclease T1 / metabolism
Ribonuclease, Pancreatic / metabolism
Shigella flexneri / genetics*
Chemical
Reg. No./Substance:
0/Bacterial Proteins; 0/DNA Primers; 0/DNA, Bacterial; 0/Escherichia coli Proteins; 0/RNA-Binding Proteins; 0/Repressor Proteins; 104042-79-7/TraM protein, bacterial; 146889-94-3/FinO protein, E coli; EC 3.1.27.3/Ribonuclease T1; EC 3.1.27.5/Ribonuclease, Pancreatic

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Non-palindromic attl sites of integrons are capable of site-specific recombination with one another ...
Next Document:  The role of ribosomal RNAs in macrolide resistance.