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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1998-6-2
pubmed:abstractText
The role of the two-component response regulator ArcA protein in the transfer of the conjugative resistance plasmid R1 was investigated using a variety of in vivo and in vitro assays. The frequency of conjugal DNA transfer of plasmid R1-16, a derepressed variant of R1, was reduced by four orders of magnitude in an Escherichia coli host with a mutation in the arcA gene. Measurements of mRNAs transcribed from key plasmid transfer genes revealed that the abundance of each of the mRNA species investigated was reduced significantly in an arcA background. Gene fusion studies with the R1 PY promoter, the major promoter of the transfer operon, and a lacZ reporter gene, indicated that arcA is required for maximal expression from this promoter. However, a stimulating effect of arcA could only be detected when the plasmid-specified positive regulator of the transfer genes, traJ, was present. Electrophoretic mobility shift assays were used to demonstrate specific binding of purified ArcA protein and a purified and phosphorylated oligohistidine-tagged ArcA (His6-ArcA) to a DNA fragment containing the PY promoter region. The binding of phosphorylated His6-ArcA to the PY promoter was further characterized by DNase I footprinting. The observed protection pattern was characteristic for ArcA acting as a transcriptional activator.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-2836
pubmed:author
pubmed:copyrightInfo
Copyright 1998 Academic Press Limited.
pubmed:issnType
Print
pubmed:day
27
pubmed:volume
277
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
309-16
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9514749-Amino Acid Sequence, pubmed-meshheading:9514749-Bacterial Outer Membrane Proteins, pubmed-meshheading:9514749-Base Sequence, pubmed-meshheading:9514749-Conjugation, Genetic, pubmed-meshheading:9514749-DNA, Bacterial, pubmed-meshheading:9514749-DNA Footprinting, pubmed-meshheading:9514749-Deoxyribonuclease I, pubmed-meshheading:9514749-Escherichia coli, pubmed-meshheading:9514749-Escherichia coli Proteins, pubmed-meshheading:9514749-Genes, Bacterial, pubmed-meshheading:9514749-Histidine, pubmed-meshheading:9514749-Molecular Sequence Data, pubmed-meshheading:9514749-Mutation, pubmed-meshheading:9514749-Operon, pubmed-meshheading:9514749-Phosphorylation, pubmed-meshheading:9514749-Promoter Regions, Genetic, pubmed-meshheading:9514749-R Factors, pubmed-meshheading:9514749-Repressor Proteins, pubmed-meshheading:9514749-Signal Transduction, pubmed-meshheading:9514749-Transcription, Genetic
pubmed:year
1998
pubmed:articleTitle
Signal transduction and bacterial conjugation: characterization of the role of ArcA in regulating conjugative transfer of the resistance plasmid R1.
pubmed:affiliation
Institut für Mikrobiologie, Universität Graz, Universitätsplatz 2, Graz, A-8010, Austria.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't