Ultraviolet light-induced plasmid-chromosome recombination in Escherichia coli: the role of recB and recF.

Gene

Department of Molecular and Cell Biology, Pennsylvania State University, University Park 16802.

Published: January 1991

Bacterial host cells of different rec genotypes were used to investigate genetic requirements of ultraviolet light (UV)-induced homologous plasmid-chromosome recombination. Plasmid DNAs which contained a wt or mutant lacY gene were irradiated with UV prior to transformation into Escherichia coli host strains which contained the complementary lacY allele. Surviving transformants were screened to determine the directions of UV-induced recombinational exchange between the bacterial and plasmid lacY genes, by assaying lactose utilization. Nonreciprocal chromosome-to-plasmid recombination was 100% dependent on the recA gene and greater than 80% dependent on the recF gene, but not dependent upon the recB gene of E. coli. In contrast, reciprocal plasmid-chromosome recombination was strictly dependent on the recA gene, greatly dependent (approx. 80%) on the recF gene, and moderately dependent on the recB gene. Nonreciprocal plasmid-to-chromosome recombination was only induced at very low frequencies, and appeared to be moderately dependent on the recB gene, but not dependent on the recF gene. UV-induced plasmid-chromosome recombination appeared to proceed by a two-step mechanism. In this model, the initial step is recF-dependent, recB-independent, and either resolves to become a nonreciprocal chromosome-to-plasmid recombinant, or proceeds to the second step. The second step is moderately recB-dependent and results in the reciprocal exchange of plasmid-chromosome sequences.

Download full-text PDF

Source
http://dx.doi.org/10.1016/0378-1119(91)90020-cDOI Listing

Publication Analysis

Top Keywords

plasmid-chromosome recombination
16
recf gene
12
dependent recb
12
recb gene
12
gene
9
escherichia coli
8
nonreciprocal chromosome-to-plasmid
8
dependent
8
dependent reca
8
reca gene
8

Similar Publications

Plasmids affect microindel mutations in Acinetobacter baylyi ADP1.

Plasmid

December 2024

Microbial Pharmacology and Population Biology Research Group, Department of Pharmacy, UiT The Arctic University of Norway, Tromsø, Norway. Electronic address:

Plasmids can impact the evolution of their hosts, e.g. due to carriage of mutagenic genes, through cross-talk with host genes or as result of SOS induction during transfer.

View Article and Find Full Text PDF

Plasmids provide an efficient vehicle for gene sharing among bacterial populations, playing a key role in bacterial evolution. Network approaches are particularly suitable to represent multipartite relationships and are useful tools to characterize plasmid-mediated gene sharing events. The bacterial family Lysobacteraceae includes plant commensal, plant pathogenic and opportunistic human pathogens for which plasmid-mediated adaptation has been reported.

View Article and Find Full Text PDF

Objectives: To investigate transferability of the poxtA-carrying plasmids in Enterococcus faecium and the mechanism of recombination that occurs during the conjugation process.

Methods: MICs were determined by broth microdilution. Transferability of the poxtA-carrying plasmids in E.

View Article and Find Full Text PDF

The transfer of DNA between Enterococcus faecium strains has been characterized both by the movement of well-defined genetic elements and by the large-scale transfer of genomic DNA fragments. In this work, we report on the whole-genome analysis of transconjugants resulting from mating events between the vancomycin-resistant E. faecium C68 strain and the vancomycin-susceptible D344RRF strain to discern the mechanism by which the transferred regions enter the recipient chromosome.

View Article and Find Full Text PDF

Horizontal transfer of genes between species is an important mechanism for bacterial genome evolution. In Escherichia coli, conjugation is the transfer from a donor (F(+)) to a recipient (F(-)) cell through cell-to-cell contact. We demonstrate what we believe to be a novel qPCR method for quantifying the transfer kinetics of the F plasmid in a population by enumerating the relative abundance of genetic loci unique to the plasmid and the chromosome.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!