Genome Research

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lespinet, O.
Right arrow Articles by Aravind, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lespinet, O.
Right arrow Articles by Aravind, L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Vol. 12, Issue 7, 1048-1059, July 2002

LETTER
The Role of Lineage-Specific Gene Family Expansion in the Evolution of Eukaryotes

Olivier Lespinet, Yuri I. Wolf, Eugene V. Koonin,1 and L. Aravind

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20894, USA

A computational procedure was developed for systematic detection of lineage-specific expansions (LSEs) of protein families in sequenced genomes and applied to obtain a census of LSEs in five eukaryotic species, the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe, the nematode Caenorhabditis elegans, the fruit fly Drosophila melanogaster, and the green plant Arabidopsis thaliana. A significant fraction of the proteins encoded in each of these genomes, up to 80% in A. thaliana, belong to LSEs. Many paralogous gene families in each of the analyzed species are almost entirely comprised of LSEs, indicating that their diversification occurred after the divergence of the major lineages of the eukaryotic crown group. The LSEs show readily discernible patterns of protein functions. The functional categories most prone to LSE are structural proteins, enzymes involved in an organism's response to pathogens and environmental stress, and various components of signaling pathways responsible for specificity, including ubiquitin ligase E3 subunits and transcription factors. The functions of several previously uncharacterized, vastly expanded protein families were predicted through in-depth protein sequence analysis, for example, small-molecule kinases and methylases that are expanded independently in the fly and in the nematode. The functions of several other major LSEs remain mysterious; these protein families are attractive targets for experimental discovery of novel, lineage-specific functions in eukaryotes. LSEs seem to be one of the principal means of adaptation and one of the most important sources of organizational and regulatory diversity in crown-group eukaryotes.

[Supplemental material is available online at ftp://ncbi.nlm.nih.gov/pub/aravind/expansions, and http://www.genome.org.]


1 Corresponding author.


12:1048-1059 ©2002 by Cold Spring Harbor Laboratory Press  ISSN 1088-9051/02 $5.00

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
GeneticsHome page
L. M. Mikhaylova, K. Nguyen, and D. I. Nurminsky
Analysis of the Drosophila melanogaster Testes Transcriptome Reveals Coordinate Regulation of Paralogous Genes
Genetics, May 1, 2008; 179(1): 305 - 315.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
H.-R. Chung, U. Lohr, and H. Jackle
Lineage-specific expansion of the Zinc Finger Associated Domain ZAD
Mol. Biol. Evol., September 1, 2007; 24(9): 1934 - 1943.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
J. R. Bishop and P. Gagneux
Evolution of carbohydrate antigens--microbial forces shaping host glycomes?
Glycobiology, May 1, 2007; 17(5): 23R - 34R.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
S. Richardt, D. Lang, R. Reski, W. Frank, and S. A. Rensing
PlanTAPDB, a Phylogeny-Based Resource of Plant Transcription-Associated Proteins
Plant Physiology, April 1, 2007; 143(4): 1452 - 1466.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. M. Babu, L. M. Iyer, S. Balaji, and L. Aravind
The natural history of the WRKY-GCM1 zinc fingers and the relationship between transcription factors and transposons
Nucleic Acids Res., December 2, 2006; 34(22): 6505 - 6520.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
S. Foret and R. Maleszka
Function and evolution of a gene family encoding odorant binding-like proteins in a social insect, the honey bee (Apis mellifera)
Genome Res., November 1, 2006; 16(11): 1404 - 1413.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J.-H. Park, L. Aravind, E. C. Wolff, J. Kaevel, Y. S. Kim, and M. H. Park
Molecular cloning, expression, and structural prediction of deoxyhypusine hydroxylase: A HEAT-repeat-containing metalloenzyme
PNAS, January 3, 2006; 103(1): 51 - 56.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
K. S. Makarova, Y. I. Wolf, S. L. Mekhedov, B. G. Mirkin, and E. V. Koonin
Ancestral paralogs and pseudoparalogs and their role in the emergence of the eukaryotic cell
Nucleic Acids Res., August 16, 2005; 33(14): 4626 - 4638.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
M. W. Hahn, T. De Bie, J. E. Stajich, C. Nguyen, and N. Cristianini
Estimating the tempo and mode of gene family evolution from comparative genomic data
Genome Res., August 1, 2005; 15(8): 1153 - 1160.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
S. Balaji, M. M. Babu, L. M. Iyer, and L. Aravind
Discovery of the principal specific transcription factors of Apicomplexa and their implication for the evolution of the AP2-integrase DNA binding domains
Nucleic Acids Res., July 21, 2005; 33(13): 3994 - 4006.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. Novatchkova, M. Wildpaner, D. Schweizer, and F. Eisenhaber
PhyloDome--visualization of taxonomic distributions of domains occurring in eukaryote protein sequence sets
Nucleic Acids Res., July 1, 2005; 33(suppl_2): W121 - W125.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
B. E. Shakhnovich, E. Deeds, C. Delisi, and E. Shakhnovich
Protein structure and evolutionary history determine sequence space topology
Genome Res., March 1, 2005; 15(3): 385 - 392.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
S. Bertrand, F. G. Brunet, H. Escriva, G. Parmentier, V. Laudet, and M. Robinson-Rechavi
Evolutionary Genomics of Nuclear Receptors: From Twenty-Five Ancestral Genes to Derived Endocrine Systems
Mol. Biol. Evol., October 1, 2004; 21(10): 1923 - 1937.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
T. J. Templeton, L. M. Iyer, V. Anantharaman, S. Enomoto, J. E. Abrahante, G.M. Subramanian, S. L. Hoffman, M. S. Abrahamsen, and L. Aravind
Comparative Analysis of Apicomplexa and Genomic Diversity in Eukaryotes
Genome Res., September 1, 2004; 14(9): 1686 - 1695.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
V. N. Babenko, I. B. Rogozin, S. L. Mekhedov, and E. V. Koonin
Prevalence of intron gain over intron loss in the evolution of paralogous gene families
Nucleic Acids Res., July 14, 2004; 32(12): 3724 - 3733.
[Abstract] [Full Text] [PDF]


Home page
Protein Sci.Home page
M. Gensheimer and A. Mushegian
Chalcone isomerase family and fold: No longer unique to plants
Protein Sci., February 1, 2004; 13(2): 540 - 544.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
N. J. Bowen, I. K. Jordan, J. A. Epstein, V. Wood, and H. L. Levin
Retrotransposons and Their Recognition of pol II Promoters: A Comprehensive Survey of the Transposable Elements From the Complete Genome Sequence of Schizosaccharomyces pombe
Genome Res., September 1, 2003; 13(9): 1984 - 1997.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Dufresne, M. Salanoubat, F. Partensky, F. Artiguenave, I. M. Axmann, V. Barbe, S. Duprat, M. Y. Galperin, E. V. Koonin, F. Le Gall, et al.
From the Cover: Genome sequence of the cyanobacterium Prochlorococcus marinus SS120, a nearly minimal oxyphototrophic genome
PNAS, August 19, 2003; 100(17): 10020 - 10025.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Genes Dev. Learn. Mem.
Protein Science RNA Genome Res.