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PMID: 2851049 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Evidence that DNA helicase I and oriT site-specific nicking are both functions of the F TraI protein.

Journal of molecular biology ·Vol. 204 ·No. 1 ·1988-11-05 ·Pages 205-9

Traxler BA, Minkley EG

Abstract

Site-specific and strand-specific nicking at the origin of transfer (oriT) of the F sex factor is the initial step in conjugal DNA metabolism. Then, DNA helicase I, the product of the traI gene, processively unwinds the plasmid from the nick site to generate the single strand of DNA that is transferred to the recipient. The nick at oriT is produced by the combined action of two Tra proteins, TraY and TraZ. The traZ gene was never precisely mapped, as no available point mutation uniquely affected TraZ-dependent oriT nicking. With several new mutations, we have demonstrated that TraZ activity is dependent upon traI DNA sequences. The simplest interpretation of this finding is that the F TraI protein is bifunctional, with DNA unwinding and site-specific DNA nicking activities.

MeSH Terms
Bacterial Proteins/genetics Binding Sites Conjugation, Genetic DNA Helicases/genetics DNA, Bacterial/metabolism Escherichia coli Proteins F Factor Genes, Bacterial Mutation Plasmids Transfection
Chemicals
Bacterial Proteins DNA, Bacterial Escherichia coli Proteins TraI protein, E coli DNA Helicases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Traxler B A
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213.
Minkley E G
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1988-11-05
Pages
205-9
Language
English
Region
England
NLM ID
2985088R
Subset
IM
Grants
NIGMS NIH HHS · GM28925 · United States
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