Molecular Biology and Evolution, Vol 15, 943-956, Copyright © 1998 by Society for Molecular Biology and Evolution
K Budin and H Philippe
The current framework of the eukaryotic phylogeny is based on the analysis
of a comprehensive set of sequences of the small subunit ribosomal RNA.
However, phylogenies based on protein-encoding genes are not completely
congruent with this picture. Since congruence between different markers is
the best tool to determine evolutionary history, we focused on Hsp70
(heat-shock protein of 70 kDa), a chaperone protein which is highly
conserved and is a potentially reliable phylogenetic marker. We used a
PCR-based approach to sequence Hsp70s in two distinct classes of Ciliates.
Seven Hsp70s were identified from Paramecium tetraurelia (Oligohymenophora)
and six Hsp70s from Euplotes aediculatus (Hypotricha), encompassing
orthologous genes for all major Hsp70 classes of Eukaryotes, i.e., those
localized in cytosol, in endoplasmic reticulum, and in mitochondria. Three
independent phylogenies of eukaryotes, based on each set of orthologous
genes, have been constructed using different tree reconstruction methods. A
significant advantage of Hsp70s is the existence of outgroups close to
Eukaryotes for these major classes, reducing the long-branch attraction
artifact due to the outgroup. The monophyly of Ciliates is supported by
good bootstrap proportions in the phylogenetic reconstructions, and this
phylum is generally a sister-group of Sporozoa, forming the expected
Alveolates clade. The Hsp70 seems to be a suitable phylogenetic marker
since it recovers all the monophyletic groups, undoubtedly defined by
morphological criteria. The Hsp70 trees are, however, notably different
from the rRNA ones and do not show two aspects of the classical topology,
i.e., the successive emergence of deeply branching groups and the vast
assembly of the major eukaryotic groups, emerging at the tip of the tree,
i.e., the "terminal crown". More precisely, the Hsp70 trees do not resolve
the relationships between the major groups of Eukaryotes with confidence,
in keeping with the hypothesis that all these groups emerged in a great
radiation that occurred at the origin of all the extant Eukaryotes.
ORIGINAL ARTICLE
New insights into the phylogeny of eukaryotes based on ciliate Hsp70 sequences
Laboratoire de Biologie Cellulaire, Universite Paris-Sud, Orsay, France.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
S. W. Roy and D. Penny A Very High Fraction of Unique Intron Positions in the Intron-Rich Diatom Thalassiosira pseudonana Indicates Widespread Intron Gain Mol. Biol. Evol., July 1, 2007; 24(7): 1447 - 1457. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Philippe, E. A. Snell, E. Bapteste, P. Lopez, P. W. H. Holland, and D. Casane Phylogenomics of Eukaryotes: Impact of Missing Data on Large Alignments Mol. Biol. Evol., September 1, 2004; 21(9): 1740 - 1752. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. A. Katz, J. G. Bornstein, E. Lasek-Nesselquist, and S. V. Muse Dramatic Diversity of Ciliate Histone H4 Genes Revealed by Comparisons of Patterns of Substitutions and Paralog Divergences Among Eukaryotes Mol. Biol. Evol., March 1, 2004; 21(3): 555 - 562. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Moreira, S. Kervestin, O. Jean-Jean, and H. Philippe Evolution of Eukaryotic Translation Elongation and Termination Factors: Variations of Evolutionary Rate and Genetic Code Deviations Mol. Biol. Evol., February 1, 2002; 19(2): 189 - 200. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Karlin and L. Brocchieri Heat shock protein 60 sequence comparisons: Duplications, lateral transfer, and mitochondrial evolution PNAS, October 10, 2000; 97(21): 11348 - 11353. [Abstract] [Full Text] [PDF] |
||||
![]() |
Testate amoebae in the Neoproterozoic Era: evidence from vase-shaped microfossils in the Chuar Group, Grand Canyon Paleobiology, September 1, 2000; 26(3): 360 - 385. |
||||
![]() |
L. Simpson, O. H. Thiemann, N. J. Savill, J. D. Alfonzo, and D. A. Maslov Evolution of RNA editing in trypanosome mitochondria PNAS, June 20, 2000; 97(13): 6986 - 6993. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. M. Sulaiman, U. M. Morgan, R. C. A. Thompson, A. A. Lal, and L. Xiao Phylogenetic Relationships of Cryptosporidium Parasites Based on the 70-Kilodalton Heat Shock Protein (HSP70) Gene Appl. Envir. Microbiol., June 1, 2000; 66(6): 2385 - 2391. [Abstract] [Full Text] |
||||
![]() |
A. Campbell, J. Mrazek, and S. Karlin Genome signature comparisons among prokaryote, plasmid, and mitochondrial DNA PNAS, August 3, 1999; 96(16): 9184 - 9189. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Karlin, L. Brocchieri, J. Mrazek, A. M. Campbell, and A. M. Spormann A chimeric prokaryotic ancestry of mitochondria and primitive eukaryotes PNAS, August 3, 1999; 96(16): 9190 - 9195. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Gray, G. Burger, and B. F. Lang Mitochondrial Evolution Science, March 5, 1999; 283(5407): 1476 - 1481. [Abstract] [Full Text] |
||||




