HOMOLOGOUS RECOMBINATION BETWEEN THE TUF GENES OF SALMONELLA-TYPHIMURIUM

Citation
F. Abdulkarim et D. Hughes, HOMOLOGOUS RECOMBINATION BETWEEN THE TUF GENES OF SALMONELLA-TYPHIMURIUM, Journal of Molecular Biology, 260(4), 1996, pp. 506-522
Citations number
86
Categorie Soggetti
Biology
ISSN journal
00222836
Volume
260
Issue
4
Year of publication
1996
Pages
506 - 522
Database
ISI
SICI code
0022-2836(1996)260:4<506:HRBTTG>2.0.ZU;2-T
Abstract
The genes coding for the translation factor EF-Tu, tufA and tufB are s eparated by over 700 kb on the circular chromosome of Salmonella typhi murium. The coding regions of these genes have 99% identity at the nuc leotide level in spite of the presumed ancient origin of the gene dupl ication. Sequence comparisons between S. typhimurium and Escherichia c oli suggest that within each species the two tuf genes are evolving in concert. Here we show that each of the S. typhimurium tuf genes can t ransfer genetic information to the other. In our genetic system the tr ansfers are seen as non-reciprocal, i.e. as gene conversion events. Ho wever, the mechanism of recombination could be reciprocal with sister chromosome segregation and selection leading to the isolation of a par ticular class of recombinant. The amount of sequence information trans ferred in individual recombination events varies, but can be close to the entire length of the gene. The recombination is RecABCD-dependent, and is opposed by MutSHLU mismatch repair. In the wild-type, this typ e of recombination occurs at a rate that is two or three orders of mag nitude greater than the nucleotide substitution rate. The rate of reco mbination differs by six orders of magnitude between a recA and a mutS strain. Mismatch repair reduces the rate of this recombination 1000-f old. The rate of recombination also differs by one order of magnitude depending on which tuf gene is donating the sequence selected for. We discuss three classes of model that could, in principle, account for t he sequence transfers: (1) tuf mRNA mediated recombination; (2) non-al lelic reciprocal recombination involving sister chromosomes; (3) non-a llelic gene conversion involving sister chromosomes, initiated by a do uble-strand break dose to one tuf gene. Although the mechanism remains to be determined, the effect on the bacterial cells is tuf gene seque nce homogenisation. This recombination phenomenon can account for the concerted evolution of the tuf genes. (C) 1996 Academic Press Limited