MBE Advance Access published online on February 9, 2005
Molecular Biology and Evolution, doi:10.1093/molbev/msi104
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1 Department of Biology, McMaster University, Life Sciences Building Room 328 1280 Main Street West, Hamilton, ON, Canada L8S 4K1
* To whom correspondence should be addressed. Possible genetic fates of a gene duplicate are silencing, redundancy, sub-functionalization, or novel function. These different fates can be realized at the DNA, RNA, or protein level, and their genetic determinants are poorly understood. We explored molecular evolution of duplicated RAG-1 genes in African clawed frogs (Xenopus and Silurana) to (1) examine the fate of paralogs of this gene at the DNA level in terms of recombination, positive selection, and gene degeneration, and - in the absence of extensive recombination among alleles at different paralogs - to (2) test phylogenetic hypotheses about the origins of polyploid species. We found that recombination between different RAG-1 paralogs is infrequent, that degeneration of some paralogs has occurred via stop codons and frameshift mutations, and that this degeneration occurred non-randomly in paralogs inherited from only one diploid progenitor species. Simulations and phylogenetic analyses of RAG-1 and mitochondrial DNA support one origin of extant tetraploids in Xenopus and at least one origin in Silurana, five allopolyploid origins of extant octoploids, and two allopolyploid origins of extant dodecaploids. In allopolyploid species, gene ancestry could potentially influence gene fate - the genetic fates of sets of genes that form complexes could be linked by a common co-evolutionary history in one of the lower ploidy ancestors.
Accepted January 25, 2005
Research Article
Evolution of RAG-1 in Polyploid Clawed Frogs
2 Department of Biological Sciences, 913 Fairchild Building, Columbia University, New York 10027, USA
3 Center for Environmental Research and Conservation and Department of Ecology, Evolution and Environmental Biology, 1200 Amsterdam Ave, Columbia University, New York 10027, USA
4 Section of Integrative Biology and Texas Memorial Museum, C0930, The University of Texas, Austin, Texas 78712-0253, USA
Ben J. Evans, E-mail: evansb{at}mcmaster.ca
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