Plant conserved non-coding sequences and paralogue evolution.

Genome duplication is a powerful evolutionary force and is arguably most prominent in plants, where several ancient whole-genome duplication events have been documented. Models of gene evolution predict that functional divergence between duplicates (subfunctionalization) is caused by the loss of regulatory elements. Studies of conserved non-coding sequences (CNSs), which are putative regulatory elements, indicate that plants have far fewer CNSs per gene than mammals, suggesting that plants have less complex regulatory mechanisms. Furthermore, a recent study of a duplicated gene pair in maize suggests that CNSs are lost in a complementary fashion, perhaps driving subfunctionalization. If subfunctionalization is common, one expects duplicate genes to diverge in expression; recent microarray analyses in Arabidopsis thalinia suggest that this is the case. Plant genomes are relatively complex on a genomic level because of the prevalence of whole-genome duplication and, paradoxically, subfunctionalization after duplication can lead to relatively simple regulatory regions on a per gene basis.

[1]  B. Birren,et al.  Proof and evolutionary analysis of ancient genome duplication in the yeast Saccharomyces cerevisiae , 2004, Nature.

[2]  Karsten Hokamp,et al.  Extensive genomic duplication during early chordate evolution , 2002, Nature Genetics.

[3]  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.

[4]  Dr. Susumu Ohno Evolution by Gene Duplication , 1970, Springer Berlin Heidelberg.

[5]  M. Gouy,et al.  Date of the monocot-dicot divergence estimated from chloroplast DNA sequence data. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[6]  Klaas Vandepoele,et al.  Evidence That Rice and Other Cereals Are Ancient Aneuploids Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.014019. , 2003, The Plant Cell Online.

[7]  M. Ashburner,et al.  Gene Ontology: tool for the unification of biology , 2000, Nature Genetics.

[8]  E Szathmáry,et al.  Molecular biology and evolution. Can genes explain biological complexity? , 2001, Science.

[9]  R. Ojeda,et al.  Discovery of tetraploidy in a mammal , 1999, Nature.

[10]  Z. Gu,et al.  Evolutionary analyses of the human genome , 2001, Nature.

[11]  Xun Gu,et al.  How much expression divergence after yeast gene duplication could be explained by regulatory motif evolution? , 2004, Trends in genetics : TIG.

[12]  T. Hartmann,et al.  Homospermidine synthase, the first pathway-specific enzyme of pyrrolizidine alkaloid biosynthesis, evolved from deoxyhypusine synthase. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[13]  V. Carginale,et al.  Adaptive evolution and functional divergence of pepsin gene family. , 2004, Gene.

[14]  Brandon S Gaut,et al.  Patterns of nucleotide substitution among simultaneously duplicated gene pairs in Arabidopsis thaliana. , 2002, Molecular biology and evolution.

[15]  Wen-Hsiung Li,et al.  Fundamentals of molecular evolution , 1990 .

[16]  Colin N. Dewey,et al.  Initial sequencing and comparative analysis of the mouse genome. , 2002 .

[17]  D. Soltis,et al.  Polyploidy: recurrent formation and genome evolution. , 1999, Trends in ecology & evolution.

[18]  A. Eyre-Walker Fundamentals of Molecular Evolution . By Li Wen-Hsiung and Graur Dan. Sinauer Associates Inc. 1991. 284 pages. £16.95. ISBN 0 87893 452 9. , 1991 .

[19]  A. Oliphant,et al.  A draft sequence of the rice genome (Oryza sativa L. ssp. japonica). , 2002, Science.

[20]  A. Paterson,et al.  Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Mouse Genome Sequencing Consortium Initial sequencing and comparative analysis of the mouse genome , 2002, Nature.

[22]  Guillaume Blanc,et al.  Widespread Paleopolyploidy in Model Plant Species Inferred from Age Distributions of Duplicate Genes , 2004, The Plant Cell Online.

[23]  A. Bashir,et al.  Conserved noncoding sequences in the grasses. , 2003, Genome research.

[24]  Roland Arnold,et al.  MIPS Arabidopsis thaliana Database (MAtDB): an integrated biological knowledge resource based on the first complete plant genome , 2002, Nucleic Acids Res..

[25]  D. G. Brown,et al.  The origins of genomic duplications in Arabidopsis. , 2000, Science.

[26]  Andrew G. Clark,et al.  Evolutionary changes in cis and trans gene regulation , 2004, Nature.

[27]  Margaret R. Thomson,et al.  Vertebrate genome evolution and the zebrafish gene map , 1998, Nature Genetics.

[28]  A. Force,et al.  Preservation of duplicate genes by complementary, degenerative mutations. , 1999, Genetics.

[29]  Guillaume Blanc,et al.  Functional Divergence of Duplicated Genes Formed by Polyploidy during Arabidopsis Evolution , 2004, The Plant Cell Online.

[30]  P. Baldi,et al.  LineUp: statistical detection of chromosomal homology with application to plant comparative genomics. , 2003, Genome research.

[31]  Michael Freeling,et al.  Genomic duplication, fractionation and the origin of regulatory novelty. , 2004, Genetics.

[32]  Joachim Schröder,et al.  Evidence that stilbene synthases have developed from chalcone synthases several times in the course of evolution , 1994, Journal of Molecular Evolution.

[33]  D. Cox,et al.  Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional. , 2004, Genome research.

[34]  I-Min A. Dubchak,et al.  Active conservation of noncoding sequences revealed by three-way species comparisons. , 2000, Genome research.

[35]  Inna Dubchak,et al.  ASDB: database of alternatively spliced genes , 1999, Nucleic Acids Res..

[36]  K. H. Wolfe,et al.  Molecular evidence for an ancient duplication of the entire yeast genome , 1997, Nature.

[37]  S. Goff,et al.  Utility and distribution of conserved noncoding sequences in the grasses , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[38]  E. Birney,et al.  Comparison of human chromosome 21 conserved nongenic sequences (CNGs) with the mouse and dog genomes shows that their selective constraint is independent of their genic environment. , 2004, Genome research.

[39]  L. Pachter,et al.  rVista for comparative sequence-based discovery of functional transcription factor binding sites. , 2002, Genome research.

[40]  The Arabidopsis Genome Initiative Analysis of the genome sequence of the flowering plant Arabidopsis thaliana , 2000, Nature.

[41]  B. Gaut,et al.  DNA sequence evidence for the segmental allotetraploid origin of maize. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[42]  Ferenc Jordán,et al.  Can Genes Explain Biological Complexity? , 2001, Science.

[43]  Klaas Vandepoele,et al.  The hidden duplication past of Arabidopsis thaliana , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[44]  S. Moose,et al.  Conserved Noncoding Sequences among Cultivated Cereal Genomes Identify Candidate Regulatory Sequence Elements and Patterns of Promoter Evolution Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.010181. , 2003, The Plant Cell Online.

[45]  Balázs Papp,et al.  Evolution of cis-regulatory elements in duplicated genes of yeast. , 2003, Trends in genetics : TIG.

[46]  Huanming Yang,et al.  A Draft Sequence of the Rice Genome (Oryza sativa L. ssp. indica) , 2002, Science.

[47]  Margaret R. Thomson,et al.  Vertebrate genome evolution and the zebrafish gene map , 1998, Nature Genetics.

[48]  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.

[49]  Brad A. Chapman,et al.  Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events , 2003, Nature.

[50]  E. Kellogg,et al.  Evolutionary history of the grasses. , 2001, Plant physiology.

[51]  T. Mitchell-Olds,et al.  Functional Divergence in Tandemly Duplicated Arabidopsis thaliana Trypsin Inhibitor Genes , 2004, Genetics.

[52]  M. Freeling Grasses as a single genetic system: reassessment 2001. , 2001, Plant physiology.

[53]  B. Gaut,et al.  Does recombination shape the distribution and evolution of tandemly arrayed genes (TAGs) in the Arabidopsis thaliana genome? , 2003, Genome research.

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

[55]  M. Feldman,et al.  Allopolyploidy-Induced Rapid Genome Evolution in the Wheat (Aegilops–Triticum) Group , 2001, The Plant Cell Online.