Mol. Biol. Evol. 20(1):62-66. 2003
DOI: 10.1093/molbev/msg006
© 2003 by the Society for Molecular Biology and Evolution. ISSN: 0737-4038
A Novel Polyubiquitin Structure in Cercozoa and Foraminifera: Evidence for a New Eukaryotic Supergroup


* Canadian Institute for Advanced Research, Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada
Département de Zoologie et Biologie Animale, University of Geneva, Geneva, Switzerland
Ubiquitin is a 76 amino acid protein with a remarkable degree of evolutionary conservation. Ubiquitin plays an essential role in a large number of eukaryotic cellular processes by targeting proteins for proteasome-mediated degradation. Most ubiquitin genes are found as head-to-tail polymers whose products are posttranslationally processed to ubiquitin monomers. We have characterized polyubuiquitin genes from the photosynthetic amoeboflagellate Chlorarachnion sp. CCMP 621 (also known as Bigelowiella natans) and found that they deviate from the canonical polyubiquitin structure in having an amino acid insertion at the junction between each monomer, suggesting that polyubiquitin processing in this organism is unique among eukaryotes. The gene structure indicates that processing likely cleaves monomers at the amino terminus of the insertion. We examined the phylogenetic distribution of the insertion by sequencing polyubiquitin genes from several other eukaryotic groups and found it to be confined to Cercozoa (including Chlorarachnion, Lotharella, Cercomonas, and Euglypha) and Foraminifera (including Reticulomyxa and Haynesina). This character strongly suggests that Cercozoa and Foraminifera are close relatives and form a new "supergroup" of eukaryotes.
Key Words: Cercozoa eukaryotes Foraminifera polyubiquitin genes
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. Z. Altin, A. Habura, and S. T. Goldstein A NEW ALLOGROMIID FORAMINIFER NIVEUS FLEXILIS NOV. GEN., NOV. SP., FROM COASTAL GEORGIA, USA: FINE STRUCTURE AND GAMETOGENESIS Journal of Foraminiferal Research, April 1, 2009; 39(2): 73 - 86. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Hampl, L. Hug, J. W. Leigh, J. B. Dacks, B. F. Lang, A. G. B. Simpson, and A. J. Roger Phylogenomic analyses support the monophyly of Excavata and resolve relationships among eukaryotic "supergroups" PNAS, March 10, 2009; 106(10): 3859 - 3864. [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] |
||||
![]() |
A. J Roger and L. A Hug The origin and diversification of eukaryotes: problems with molecular phylogenetics and molecular clock estimation Phil Trans R Soc B, June 29, 2006; 361(1470): 1039 - 1054. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Flakowski, I. Bolivar, J. Fahrni, and J. Pawlowski ACTIN PHYLOGENY OF FORAMINIFERA Journal of Foraminiferal Research, April 1, 2005; 35(2): 93 - 102. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Arisue, M. Hasegawa, and T. Hashimoto Root of the Eukaryota Tree as Inferred from Combined Maximum Likelihood Analyses of Multiple Molecular Sequence Data Mol. Biol. Evol., March 1, 2005; 22(3): 409 - 420. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Bass and T. Cavalier-Smith Phylum-specific environmental DNA analysis reveals remarkably high global biodiversity of Cercozoa (Protozoa) Int J Syst Evol Microbiol, November 1, 2004; 54(6): 2393 - 2404. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. I. Nikolaev, C. Berney, J. F. Fahrni, I. Bolivar, S. Polet, A. P. Mylnikov, V. V. Aleshin, N. B. Petrov, and J. Pawlowski From the Cover: The twilight of Heliozoa and rise of Rhizaria, an emerging supergroup of amoeboid eukaryotes PNAS, May 25, 2004; 101(21): 8066 - 8071. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Longet, J. M. Archibald, P. J. Keeling, and J. Pawlowski Foraminifera and Cercozoa share a common origin according to RNA polymerase II phylogenies Int J Syst Evol Microbiol, November 1, 2003; 53(6): 1735 - 1739. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Pawlowski, M. Holzmann, C. Berney, J. Fahrni, A. J. Gooday, T. Cedhagen, A. Habura, and S. S. Bowser The evolution of early Foraminifera PNAS, September 30, 2003; 100(20): 11494 - 11498. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Archibald, M. B. Rogers, M. Toop, K.-i. Ishida, and P. J. Keeling Lateral gene transfer and the evolution of plastid-targeted proteins in the secondary plastid-containing alga Bigelowiella natans PNAS, June 24, 2003; 100(13): 7678 - 7683. [Abstract] [Full Text] [PDF] |
||||




