Analysis of the sequence and gene products of the transfer region of the F sex factor.
- 1 June 1994
- journal article
- research article
- Vol. 58 (2) , 162-210
Abstract
Bacterial conjugation results in the transfer of DNA of either plasmid or chromosomal origin between microorganisms. Transfer begins at a defined point in the DNA sequence, usually called the origin of transfer (oriT). The capacity of conjugative DNA transfer is a property of self-transmissible plasmids and conjugative transposons, which will mobilize other plasmids and DNA sequences that include a compatible oriT locus. This review will concentrate on the genes required for bacterial conjugation that are encoded within the transfer region (or regions) of conjugative plasmids. One of the best-defined conjugation systems is that of the F plasmid, which has been the paradigm for conjugation systems since it was discovered nearly 50 years ago. The F transfer region (over 33 kb) contains about 40 genes, arranged contiguously. These are involved in the synthesis of pili, extracellular filaments which establish contact between donor and recipient cells; mating-pair stabilization; prevention of mating between similar donor cells in a process termed surface exclusions; DNA nicking and transfer during conjugation; and the regulation of expression of these functions. This review is a compendium of the products and other features found in the F transfer region as well as a discussion of their role in conjugation. While the genetics of F transfer have been described extensively, the mechanism of conjugation has proved elusive, in large part because of the low levels of expression of the pilus and the numerous envelope components essential for F plasmid transfer. The advent of molecular genetic techniques has, however, resulted in considerable recent progress. This summary of the known properties of the F transfer region is provided in the hope that it will form a useful basis for future comparison with other conjugation systems.This publication has 100 references indexed in Scilit:
- Mechanism of killer gene activation. Antisense RNA-dependent RNase III cleavage ensures rapid turn-over of the stable Hok, SrnB and PndA effector messenger RNAsJournal of Molecular Biology, 1992
- Characterization of the F plasmid mating aggregation gene traN and of a new F transfer region locus trbEJournal of Molecular Biology, 1992
- Regulation of the F plasmid tra Y promoter in Escherichia coli K12 as a function of sequence contextJournal of Molecular Biology, 1991
- Regulation of the F plasmid tra Y promoter in Escherichia coli by host and plasmid factorsJournal of Molecular Biology, 1991
- Mechanism of post‐segregational killing by the hoklsok system of plasmid R1: sok antisense RNA regulates formation of a hok mRNA species correlated with killing of plasmid‐free cellsMolecular Microbiology, 1990
- The mobilization and origin of transfer regions of a Thiobacillus ferrooxidans plasmid: relatedness to plasmids RSF1010 and pSC101Molecular Microbiology, 1990
- Nucleotide sequence of the promoter-distal region of thetra operon of plasmid R100, includingtraI (DNA helicase I) andtraD genesJournal of Molecular Biology, 1990
- Nucleotide sequence of the F plasmid gene, traC, and identification of its productGene, 1990
- X-ray diffraction and electron microscope studies on the structure of bacterial F piliJournal of Molecular Biology, 1979
- The transcriptional control of fertility in F-like plasmidsJournal of Molecular Biology, 1977