BackgroundThe recA/RAD51 gene family encodes a diverse set of recombinase proteins that affect homologous recombination, DNA-repair, and genome stability. The recA gene family is expressed across all three domains of life - Eubacteria, Archaea, and Eukaryotes - and even in some viruses. To date, efforts to resolve the deep evolutionary origins of this ancient protein family have been hindered by the high sequence divergence between paralogous groups (i.e. ~30% average pairwise identity).ResultsThrough large taxon sampling and the use of a phylogenetic algorithm designed for inferring evolutionary events in highly divergent paralogs, we obtained a robust, parsimonious and more refined phylogenetic history of the recA/RAD51 superfamily.ConclusionsIn summary, our model for the evolution of recA/RAD51 family provides a better understanding of the ancient origin of recA proteins and the multiple events that lead to the diversification of recA homologs in eukaryotes, including the discovery of additional RAD51 sub-families.
Reevaluation of the evolutionary events within recA/RAD51 phylogeny
S. Chintapalli,G. Bhardwaj,Jagadish Babu,Loukia Hadjiyianni,Yoojin Hong,George K Todd,Casey A. Boosalis,Zhenhai Zhang,Xiaofan Zhou,Hong Ma,A. Anishkin,D. V. van Rossum,R. Patterson
Published 2013 in BMC Genomics
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- Publication year
2013
- Venue
BMC Genomics
- Publication date
2013-04-10
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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