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Evolutionary diversification of an ancient gene family (rhs) through C-terminal displacement.

Authors :
Jackson AP
Thomas GH
Parkhill J
Thomson NR
Source :
BMC genomics [BMC Genomics] 2009 Dec 07; Vol. 10, pp. 584. Date of Electronic Publication: 2009 Dec 07.
Publication Year :
2009

Abstract

Background: Rhs genes are prominent features of bacterial genomes that have previously been implicated in genomic rearrangements in E. coli. By comparing rhs repertoires across the Enterobacteriaceae, this study provides a robust explanation of rhs diversification and evolution, and a mechanistic model of how rhs diversity is gained and lost.<br />Results: Rhs genes are ubiquitous and comprise six structurally distinct lineages within the Enterobacteriaceae. There is considerable intergenomic variation in rhs repertoire; for instance, in Salmonella enterica, rhs are restricted to mobile elements, while in Escherichia coli one rhs lineage has diversified through transposition as older lineages have been deleted. Overall, comparative genomics reveals frequent, independent gene gains and losses, as well as occasional lateral gene transfer, in different genera. Furthermore, we demonstrate that Rhs 'core' domains and variable C-termini are evolutionarily decoupled, and propose that rhs diversity is driven by homologous recombination with circular intermediates. Existing C-termini are displaced by laterally acquired alternatives, creating long arrays of dissociated 'tips' that characterize the appearance of rhs loci.<br />Conclusion: Rhs repertoires are highly dynamic among Enterobacterial genomes, due to repeated gene gains and losses. In contrast, the primary structures of Rhs genes are evolutionarily conserved, indicating that rhs sequence diversity is driven, not by rapid mutation, but by the relatively slow evolution of novel core/tip combinations. Hence, we predict that a large pool of dissociated rhs C-terminal tips exists episomally and these are potentially transmitted across taxonomic boundaries.

Details

Language :
English
ISSN :
1471-2164
Volume :
10
Database :
MEDLINE
Journal :
BMC genomics
Publication Type :
Academic Journal
Accession number :
19968874
Full Text :
https://doi.org/10.1186/1471-2164-10-584