Abstract
The transfer operon of the F plasmid is positively regulated by the traJ gene product, expression of which, in turn, is regulated by both an antisense RNA, FinP, and the FinO protein (the FinOP system). A finP- F plasmid, pSFL20, was constructed by site-directed mutagenesis and was found to produce wild-type levels of pili encoded by the transfer operon. Transcription of the traJ gene was decreased by a factor of 3-5 fold in the presence of FinOP with no accumulation of a stable RNA duplex between the FinP RNA and the portion of the traJ mRNA which is complementary to finP. Stabilization of FinP RNA by FinO occurs in the absence of traJ transcripts, suggesting that FinO may interact directly with FinP to prevent its degradation.
MeSH Terms
Bacterial Outer Membrane Proteins/genetics,metabolism
Bacterial Proteins/metabolism
Base Sequence
Cloning, Molecular
DNA, Bacterial
Endoribonucleases/metabolism
Escherichia coli/genetics,metabolism
Escherichia coli Proteins
F Factor
Gene Expression Regulation, Bacterial
Half-Life
Molecular Sequence Data
Mutagenesis, Site-Directed
Operon
Promoter Regions, Genetic
RNA, Antisense/metabolism
RNA-Binding Proteins
Repressor Proteins
Transcription, Genetic
Chemicals
Bacterial Outer Membrane Proteins
Bacterial Proteins
DNA, Bacterial
Escherichia coli Proteins
RNA, Antisense
RNA-Binding Proteins
Repressor Proteins
TraJ protein, E coli
TraJ protein, bacteria
FinO protein, E coli
Endoribonucleases
ribonuclease E
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lee S H
Department of Biochemistry, University of Alberta, Edmonton, Canada.
Frost L S
Paranchych W
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