First published online June 18, 2004; 10.1105/tpc.021345
The Plant Cell 16:1667-1678 (2004)
© 2004 American Society of Plant Biologists
Widespread Paleopolyploidy in Model Plant Species Inferred from Age Distributions of Duplicate Genes
Guillaume Blanca,b,1 and
Kenneth H. Wolfea
a Department of Genetics, Smurfit Institute, University of Dublin, Trinity College, Dublin 2, Ireland
b Laboratoire Information Génomique et Structurale, Centre National de la Recherche Scientifique UPR 2589, 13402 Marseille Cedex 20, France
1 To whom correspondence should be addressed. E-mail g_blanc{at}univ-perp.fr; fax 33-4-91164549.
It is often anticipated that many of today's diploid plant species are in fact paleopolyploids. Given that an ancient large-scale duplication will result in an excess of relatively old duplicated genes with similar ages, we analyzed the timing of duplication of pairs of paralogous genes in 14 model plant species. Using EST contigs (unigenes), we identified pairs of paralogous genes in each species and used the level of synonymous nucleotide substitution to estimate the relative ages of gene duplication. For nine of the investigated species (wheat [Triticum aestivum], maize [Zea mays], tetraploid cotton [Gossypium hirsutum], diploid cotton [G. arboretum], tomato [Lycopersicon esculentum], potato [Solanum tuberosum], soybean [Glycine max], barrel medic [Medicago truncatula], and Arabidopsis thaliana), the age distributions of duplicated genes contain peaks corresponding to short evolutionary periods during which large numbers of duplicated genes were accumulated. Large-scale duplications (polyploidy or aneuploidy) are strongly suspected to be the cause of these temporal peaks of gene duplication. However, the unusual age profile of tandem gene duplications in Arabidopsis indicates that other scenarios, such as variation in the rate at which duplicated genes are deleted, must also be considered.
Related articles in Plant Cell:
- Two Genomes Are Better Than One: Widespread Paleopolyploidy in Plants and Evolutionary Effects
- Nancy A. Eckardt
Plant Cell 2004 16: 1647-1649.
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M. E. Schranz and T. Mitchell-Olds
Independent Ancient Polyploidy Events in the Sister Families Brassicaceae and Cleomaceae
PLANT CELL,
May 1, 2006;
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K. D. Crow and G. P. Wagner
What Is the Role of Genome Duplication in the Evolution of Complexity and Diversity?
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May 1, 2006;
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C. Maher, L. Stein, and D. Ware
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April 1, 2006;
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A. J. Windsor, M. E. Schranz, N. Formanova, S. Gebauer-Jung, J. G. Bishop, D. Schnabelrauch, J. Kroymann, and T. Mitchell-Olds
Partial Shotgun Sequencing of the Boechera stricta Genome Reveals Extensive Microsynteny and Promoter Conservation with Arabidopsis.
Plant Physiology,
April 1, 2006;
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J. G. Walling, R. Shoemaker, N. Young, J. Mudge, and S. Jackson
Chromosome-Level Homeology in Paleopolyploid Soybean (Glycine max) Revealed Through Integration of Genetic and Chromosome Maps
Genetics,
March 1, 2006;
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B. A. Chapman, J. E. Bowers, F. A. Feltus, and A. H. Paterson
Buffering of crucial functions by paleologous duplicated genes may contribute cyclicality to angiosperm genome duplication
PNAS,
February 21, 2006;
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J. M. Duarte, L. Cui, P. K. Wall, Q. Zhang, X. Zhang, J. Leebens-Mack, H. Ma, N. Altman, and C. W. dePamphilis
Expression Pattern Shifts Following Duplication Indicative of Subfunctionalization and Neofunctionalization in Regulatory Genes of Arabidopsis
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February 1, 2006;
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J. L. Shultz, D. Kurunam, K. Shopinski, M. J. Iqbal, S. Kazi, K. Zobrist, R. Bashir, S. Yaegashi, N. Lavu, A. J. Afzal, et al.
The Soybean Genome Database (SoyGD): a browser for display of duplicated, polyploid, regions and sequence tagged sites on the integrated physical and genetic maps of Glycine max
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January 1, 2006;
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M. Bevan and S. Walsh
The Arabidopsis genome: A foundation for plant research
Genome Res.,
December 1, 2005;
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Y. Jiao, L. Ma, E. Strickland, and X. W. Deng
Conservation and Divergence of Light-Regulated Genome Expression Patterns during Seedling Development in Rice and Arabidopsis
PLANT CELL,
December 1, 2005;
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M. Mondragon-Palomino and B. S. Gaut
Gene Conversion and the Evolution of Three Leucine-Rich Repeat Gene Families in Arabidopsis thaliana
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December 1, 2005;
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J. Rong, J. E. Bowers, S. R. Schulze, V. N. Waghmare, C. J. Rogers, G. J. Pierce, H. Zhang, J. C. Estill, and A. H. Paterson
Comparative genomics of Gossypium and Arabidopsis: Unraveling the consequences of both ancient and recent polyploidy
Genome Res.,
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Y. Fu, S. J. Emrich, L. Guo, T.-J. Wen, D. A. Ashlock, S. Aluru, and P. S. Schnable
Quality assessment of maize assembled genomic islands (MAGIs) and large-scale experimental verification of predicted genes
PNAS,
August 23, 2005;
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B. E. Pfeil, J. A. Schlueter, R. C. Shoemaker, and J. J. Doyle
Placing Paleopolyploidy in Relation to Taxon Divergence: A Phylogenetic Analysis in Legumes Using 39 Gene Families
Syst Biol,
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Y. Jiao, P. Jia, X. Wang, N. Su, S. Yu, D. Zhang, L. Ma, Q. Feng, Z. Jin, L. Li, et al.
A Tiling Microarray Expression Analysis of Rice Chromosome 4 Suggests a Chromosome-Level Regulation of Transcription
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June 1, 2005;
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Y. Zhang, Y. Wu, Y. Liu, and B. Han
Computational Identification of 69 Retroposons in Arabidopsis
Plant Physiology,
June 1, 2005;
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L. M. Zahn, J. Leebens-Mack, C. W. dePamphilis, H. Ma, and G. Theissen
To B or Not to B a Flower: The Role of DEFICIENS and GLOBOSA Orthologs in the Evolution of the Angiosperms
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S. Maere, S. De Bodt, J. Raes, T. Casneuf, M. Van Montagu, M. Kuiper, and Y. Van de Peer
Modeling gene and genome duplications in eukaryotes
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April 12, 2005;
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V. Hecht, F. Foucher, C. Ferrandiz, R. Macknight, C. Navarro, J. Morin, M. E. Vardy, N. Ellis, J. P. Beltran, C. Rameau, et al.
Conservation of Arabidopsis Flowering Genes in Model Legumes
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K. L. Adams, R. Percifield, and J. F. Wendel
Organ-Specific Silencing of Duplicated Genes in a Newly Synthesized Cotton Allotetraploid
Genetics,
December 1, 2004;
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N. A. Eckardt
Two Genomes Are Better Than One: Widespread Paleopolyploidy in Plants and Evolutionary Effects
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