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pubmed-article:15975830pubmed:abstractTextDespite its great diversity and biomedical importance, the rodent subfamily Murinae is poorly resolved phylogenetically. We present the first cladistic analysis sampling multiple representatives of most major groups based on DNA sequence for three nuclear (GHR, RAG1, and AP5) and one mitochondrial (COII and parts of COI and ATPase 8) fragments. Analyzed separately, the four partitions agree broadly with each other and the combined analysis. The basal split is between a clade of Philippine Old Endemics and all remaining murines. Within the latter, rapid radiation led to at least seven geographically distinct lineages, including a Southeast Asian Rattus clade; a diverse Australo-Papuan and Philippine clade; an African arvicanthine group including the otomyines; an African Praomys group; and three independent genera from Africa and Asia, Mus, Apodemus, and Malacomys. The murines appear to have originated in Southeast Asia and then rapidly expanded across all of the Old World. Both nuclear exons provide robust support at all levels. In contrast, the bootstrap proportions from mitochondrial data decline rapidly with increasing depth in the tree, together suggesting that nuclear genes may be more useful even for relatively recent divergences (< 10MYA).lld:pubmed
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pubmed-article:15975830pubmed:pagination370-88lld:pubmed
pubmed-article:15975830pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15975830pubmed:articleTitleMultigene phylogeny of the Old World mice, Murinae, reveals distinct geographic lineages and the declining utility of mitochondrial genes compared to nuclear genes.lld:pubmed
pubmed-article:15975830pubmed:affiliationDepartment of Biological Science, Florida State University, Tallahassee, FL 32306-1100, USA. steppan@bio.fsu.edulld:pubmed
pubmed-article:15975830pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15975830pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:15975830pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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