MBE Advance Access originally published online on September 8, 2005
Molecular Biology and Evolution 2006 23(1):93-106; doi:10.1093/molbev/msj011
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Article |
The Protistan Origins of Animals and Fungi
Department of Biology, University of York, Heslington, York, United Kingdom
E-mail: slb14{at}york.ac.uk.
Recent molecular studies suggest that Opisthokonta, the eukaryotic supergroup including animals and fungi, should be expanded to include a diverse collection of primitively single-celled eukaryotes previously classified as Protozoa. These taxa include corallochytreans, nucleariids, ministeriids, choanoflagellates, and ichthyosporeans. Assignment of many of these taxa to Opisthokonta remains uncorroborated as it is based solely on small subunit ribosomal RNA trees lacking resolution and significant bootstrap support for critical nodes. Therefore, important details of the phylogenetic relationships of these putative opisthokonts with each other and with animals and fungi remain unclear. We have sequenced elongation factor 1-alpha (EF-1
), actin, ß-tubulin, and HSP70, and/or
-tubulin from representatives of each of the proposed protistan opisthokont lineages, constituting the first protein-coding gene data for some of them. Our results show that members of all opisthokont protist groups encode a
12-amino acid insertion in EF-1
, previously found exclusively in animals and fungi. Phylogenetic analyses of combined multigene data sets including a diverse set of opisthokont and nonopisthokont taxa place all of the proposed opisthokont protists unequivocally in an exclusive clade with animals and fungi. Within this clade, the nucleariid appears as the closest sister taxon to fungi, while the corallochytrean and ichthyosporean form a group which, together with the ministeriid and choanoflagellates, form two to three separate sister lineages to animals. These results further establish Opisthokonta as a bona fide taxonomic group and suggest that any further testing of the legitimacy of this taxon should, at the least, include data from opisthokont protists. Our results also underline the critical position of these "animal-fungal allies" with respect to the origin and early evolution of animals and fungi.
Key Words: Opisthokonta animals fungi evolution protists holozoa
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Elias The Guanine Nucleotide Exchange Factors Sec2 and PRONE: Candidate Synapomorphies for the Opisthokonta and the Archaeplastida Mol. Biol. Evol., August 1, 2008; 25(8): 1526 - 1529. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.-M. Bourbon Comparative genomics supports a deep evolutionary origin for the large, four-module transcriptional mediator complex Nucleic Acids Res., July 1, 2008; 36(12): 3993 - 4008. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Fahey, C. Larroux, B. J. Woodcroft, and B. M. Degnan Does the High Gene Density in the Sponge NK Homeobox Gene Cluster Reflect Limited Regulatory Capacity? Biol. Bull., June 1, 2008; 214(3): 205 - 217. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Li, S. L. Young, N. King, and W. T. Miller Signaling Properties of a Non-metazoan Src Kinase and the Evolutionary History of Src Negative Regulation J. Biol. Chem., May 30, 2008; 283(22): 15491 - 15501. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. L. Wheeler, D. Miranda-Saavedra, and G. J. Barton Genome Analysis of the Unicellular Green Alga Chlamydomonas reinhardtii Indicates an Ancient Evolutionary Origin for Key Pattern Recognition and Cell-Signaling Protein Families Genetics, May 1, 2008; 179(1): 193 - 197. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Larroux, G. N. Luke, P. Koopman, D. S. Rokhsar, S. M. Shimeld, and B. M. Degnan Genesis and Expansion of Metazoan Transcription Factor Gene Classes Mol. Biol. Evol., May 1, 2008; 25(5): 980 - 996. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Ruiz-Trillo, A. J. Roger, G. Burger, M. W. Gray, and B. F. Lang A Phylogenomic Investigation into the Origin of Metazoa Mol. Biol. Evol., April 1, 2008; 25(4): 664 - 672. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Abedin and N. King The Premetazoan Ancestry of Cadherins Science, February 15, 2008; 319(5865): 946 - 948. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Davila Lopez and T. Samuelsson Early evolution of histone mRNA 3' end processing RNA, January 1, 2008; 14(1): 1 - 10. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Coronado, S. Mneimneh, S. L. Epstein, W.-G. Qiu, and P. N. Lipke Conserved Processes and Lineage-Specific Proteins in Fungal Cell Wall Evolution Eukaryot. Cell, December 1, 2007; 6(12): 2269 - 2277. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Slot, K. N. Hallstrom, P. B. Matheny, and D. S. Hibbett Diversification of NRT2 and the Origin of Its Fungal Homolog Mol. Biol. Evol., August 1, 2007; 24(8): 1731 - 1743. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Kim, A. G. B. Simpson, and L. E. Graham Evolutionary Relationships of Apusomonads Inferred from Taxon-Rich Analyses of 6 Nuclear Encoded Genes Mol. Biol. Evol., December 1, 2006; 23(12): 2455 - 2466. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Blackwell, D. S. Hibbett, J. W. Taylor, and J. W. Spatafora Research Coordination Networks: a phylogeny for kingdom Fungi (Deep Hypha) Mycologia, November 1, 2006; 98(6): 829 - 837. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Burki and J. Pawlowski Monophyly of Rhizaria and Multigene Phylogeny of Unicellular Bikonts Mol. Biol. Evol., October 1, 2006; 23(10): 1922 - 1930. [Abstract] [Full Text] [PDF] |
||||








