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dc.contributor.authorParfrey, Laura Wegener
dc.contributor.authorGrant, Jessica
dc.contributor.authorTekle, Yonas I.
dc.contributor.authorLasek-Nesselquist, Erica
dc.contributor.authorMorrison, Hilary G.
dc.contributor.authorSogin, Mitchell L.
dc.contributor.authorPatterson, David J.
dc.contributor.authorKatz, Laura A.
dc.date.accessioned2010-11-15T15:29:05Z
dc.date.available2011-07-23T08:26:05Z
dc.date.issued2010-06-01
dc.identifier.urihttp://hdl.handle.net/1912/4086
dc.descriptionAuthor Posting. © The Authors, 2010. This is the author's version of the work. It is posted here by permission of Oxford University Press for personal use, not for redistribution. The definitive version was published in Systematic Biology 59 (2010): 518-533, doi:10.1093/sysbio/syq037.en_US
dc.description.abstractAn accurate reconstruction of the eukaryotic tree of life is essential to identify the innovations underlying the diversity of microbial and macroscopic (e.g. plants and animals) eukaryotes. Previous work has divided eukaryotic diversity into a small number of high-level ‘supergroups’, many of which receive strong support in phylogenomic analyses. However, the abundance of data in phylogenomic analyses can lead to highly supported but incorrect relationships due to systematic phylogenetic error. Further, the paucity of major eukaryotic lineages (19 or fewer) included in these genomic studies may exaggerate systematic error and reduces power to evaluate hypotheses. Here, we use a taxon-rich strategy to assess eukaryotic relationships. We show that analyses emphasizing broad taxonomic sampling (up to 451 taxa representing 72 major lineages) combined with a moderate number of genes yield a well-resolved eukaryotic tree of life. The consistency across analyses with varying numbers of taxa (88-451) and levels of missing data (17-69%) supports the accuracy of the resulting topologies. The resulting stable topology emerges without the removal of rapidly evolving genes or taxa, a practice common to phylogenomic analyses. Several major groups are stable and strongly supported in these analyses (e.g. SAR, Rhizaria, Excavata), while the proposed supergroup ‘Chromalveolata’ is rejected. Further, extensive instability among photosynthetic lineages suggests the presence of systematic biases including endosymbiotic gene transfer from symbiont (nucleus or plastid) to host. Our analyses demonstrate that stable topologies of ancient evolutionary relationships can be achieved with broad taxonomic sampling and a moderate number of genes. Finally, taxonrich analyses such as presented here provide a method for testing the accuracy of relationships that receive high bootstrap support in phylogenomic analyses and enable placement of the multitude of lineages that lack genome scale data.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.relation.urihttp://dx.doi.org/10.1093/sysbio/syq037
dc.subjectMicrobial eukaryotesen_US
dc.subjectSupergroupsen_US
dc.subjectTaxon samplingen_US
dc.subjectRhizariaen_US
dc.subjectSystematic erroren_US
dc.subjectExcavataen_US
dc.titleBroadly sampled multigene analyses yield a well-resolved eukaryotic tree of lifeen_US
dc.typePreprinten_US


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