Polyploidy: genome obesity and its consequences.

Polyploidy is a major evolutionary feature of many plants and some animals (Grant, 1981; Otto & Whitton, 2000). Allopolyploids (e.g. wheat, cotton, and canola) were formed by combination of two or more distinct genomes, whereas autopolyploids (e.g. potato, sugarcane, and banana) resulted from duplication of a single genome. Both allopolyploids and autopolyploids are prevalent in nature (Tate et al., 2004). Recent research has shown that polyploid genomes may undergo rapid changes in genome structure and function via genetic and epigenetic changes (Fig. 1) (Levy & Feldman, 2002; Osborn et al., 2003; Chen, 2007). The former include chromosomal rearrangements (e.g. translocation, deletion, and transposition) and DNA sequence elimination and mutations, whereas epigenetic modifications (chromatin and RNA-mediated pathways) give rise to gene expression changes that are not associated with changes in DNA sequence. Over time, polyploids may become ‘diploidized’ so that they behave like diploids cytogenetically and genetically. Comparative and genome sequence analyses indicate that many plant species, including maize, rice, poplar, and Arabidopsis, are recent or ancient diploidized (paleo-) polyploids. Fig. 1 Diagram of allopolyploid formation and evolution The consequences of polyploidy have been of long-standing interest in genetics, evolution, and systematics (Wendel, 2000; Soltis et al., 2003). Research interest in polyploids has been renewed in the past decade following the discovery of multiple origins and patterns of polyploid formation (Soltis et al., 2003) and rapid genetic changes in resynthesized allotetraploids in Brassica (Song et al., 1995) and wheat (Feldman et al., 1997). Rapid technological advances have also facilitated genomic-scale investigation of polyploids and hybrids (Wang et al., 2006). Many ongoing studies are focused on investigation of: (i) the evolutionary consequence of gene and genome duplications in polyploids; (ii) genomic and gene expression changes in resynthesized allotetraploids; (iii) genetic and gene expression variation in natural populations of polyploids; and (iv) comparison of genetic and gene expression changes in resynthesized and natural polyploids (Wendel, 2000; Osborn et al., 2003; Soltis et al., 2003; Comai, 2005; Chen, 2007). The presentations given at the Polyploidy workshop, Plant and Animal Genome XV Conference (http://www.intl-pag.org/), reflected these current research themes, reporting on ancient polyploidy events in Glycine, expression evolution of duplicate genes in Arabidopsis, gene expression changes in resynthesized Brassica and wheat allopolyploids, hybridization barriers in Arabidopsis, and tissue-specific and stress-induced expression patterns of duplicate genes in cotton and hybrid Populus. ‘… expression of duplicate genes in response to developmental programs is more strongly correlated than that of duplicate genes in response to environmental stresses, suggesting rapid evolution of duplicate genes in response to external factors’

[1]  L. Rieseberg,et al.  Plant Speciation , 2007, Science.

[2]  Z. Chen,et al.  Genetic and epigenetic mechanisms for gene expression and phenotypic variation in plant polyploids. , 2007, Annual review of plant biology.

[3]  G. Kema,et al.  MgHog1 regulates dimorphism and pathogenicity in the fungal wheat pathogen Mycosphaerella graminicola. , 2006, Molecular plant-microbe interactions : MPMI.

[4]  R. Shoemaker,et al.  Sequence Conservation of Homeologous Bacterial Artificial Chromosomes and Transcription of Homeologous Genes in Soybean (Glycine max L. Merr.) , 2006, Genetics.

[5]  N. Talbot,et al.  Evolution of Filamentous Plant Pathogens: Gene Exchange across Eukaryotic Kingdoms , 2006, Current Biology.

[6]  Laura Baxter,et al.  Phytophthora Genome Sequences Uncover Evolutionary Origins and Mechanisms of Pathogenesis , 2006, Science.

[7]  U. Sagaram,et al.  The putative monomeric G-protein GBP1 is negatively associated with fumonisin B production in Fusarium verticillioides. , 2006, Molecular plant pathology.

[8]  S. Kamoun A catalogue of the effector secretome of plant pathogenic oomycetes. , 2006, Annual review of phytopathology.

[9]  Caroline Josefsson,et al.  Parent-Dependent Loss of Gene Silencing during Interspecies Hybridization , 2006, Current Biology.

[10]  R W Doerge,et al.  Genomewide Nonadditive Gene Regulation in Arabidopsis Allotetraploids , 2006, Genetics.

[11]  R. Gregory The evolution of the genome , 2005 .

[12]  James E. Galagan,et al.  Genomics of the fungal kingdom: Insights into eukaryotic biology , 2005 .

[13]  Luca Comai,et al.  The advantages and disadvantages of being polyploid , 2005, Nature Reviews Genetics.

[14]  L. Lukens,et al.  Flowering time divergence and genomic rearrangements in resynthesized Brassica polyploids (Brassicaceae) , 2004 .

[15]  S. Kroken,et al.  Phylogenomic analysis of type I polyketide synthase genes in pathogenic and saprobic ascomycetes , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Douglas E. Soltis,et al.  Advances in the study of polyploidy since Plant speciation , 2003 .

[17]  R. Scott,et al.  The Basis of Natural and Artificial Postzygotic Hybridization Barriers in Arabidopsis Species Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.010496. , 2003, The Plant Cell Online.

[18]  Jonathan F. Wendel,et al.  Genes duplicated by polyploidy show unequal contributions to the transcriptome and organ-specific reciprocal silencing , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[19]  K. Eversole,et al.  A plant-associated microbe genome initiative. , 2003, Phytopathology.

[20]  Vincent Colot,et al.  Understanding mechanisms of novel gene expression in polyploids. , 2003, Trends in genetics : TIG.

[21]  K. Hokamp,et al.  A recent polyploidy superimposed on older large-scale duplications in the Arabidopsis genome. , 2003, Genome research.

[22]  M. Feldman,et al.  The Impact of Polyploidy on Grass Genome Evolution , 2002, Plant Physiology.

[23]  S. Kamoun,et al.  Agricultural Microbes Genome 2: First Glimpses into the Genomes of Plant-Associated Microbes , 2001, Plant Cell.

[24]  G. Segal,et al.  Rapid elimination of low-copy DNA sequences in polyploid wheat: a possible mechanism for differentiation of homoeologous chromosomes. , 1997, Genetics.

[25]  Z. Chen,et al.  Transcriptional analysis of nucleolar dominance in polyploid plants: biased expression/silencing of progenitor rRNA genes is developmentally regulated in Brassica. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[26]  P. Lu,et al.  Rapid genome change in synthetic polyploids of Brassica and its implications for polyploid evolution. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[27]  S. Langlois,et al.  Parental origin of triploidy in human fetuses: evidence for genomic imprinting , 1993, Human Genetics.

[28]  D. Soltis,et al.  Polyploidy in Plants , 2005 .

[29]  Jonathan F. Wendel,et al.  Genome evolution in polyploids , 2004, Plant Molecular Biology.

[30]  S. Otto,et al.  Polyploid incidence and evolution. , 2000, Annual review of genetics.

[31]  A. Force,et al.  The probability of duplicate gene preservation by subfunctionalization. , 2000, Genetics.