Population and evolutionary dynamics of Helitron transposable elements in Arabidopsis thaliana.

Helitrons, a recently discovered superfamily of DNA transposons that capture host gene fragments, constitute up to 2% of the Arabidopsis thaliana genome. In this study, we identified 565 insertions of a family of nonautonomous Helitrons, known as Basho elements. We aligned subsets of these elements, estimated their phylogenetic relationships, and used branch lengths to yield insight into the age of each Basho insertion. The age distribution suggests that 87% of Bashos inserted within 5 Myr, subsequent to the divergence between A. thaliana and its sister species Arabidopsis lyrata. We screened 278 of these insertions for their presence or absence in a sample of 47 A. thaliana accessions. With both phylogenetic and population frequency data, we investigated the effects of gene density, recombination rate, and element length on Basho persistence. Our analyses suggested that longer Basho copies are less likely to persist in the genome, consistent with selection against the deleterious effects of ectopic recombination between Basho elements. Furthermore, we determined that 39% of Basho elements contain fragments of expressed protein-coding genes, but all of these fragments were explained by only 5 gene-capture events. Overall, the picture of A. thaliana Helitron evolution is one of rapid expansion, relatively few gene-capture events, and weak selection correlated with element length.

[1]  M. Kimura,et al.  The neutral theory of molecular evolution. , 1983, Scientific American.

[2]  S Wright,et al.  Transposon diversity in Arabidopsis thaliana. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[3]  S. Wessler,et al.  Recent, extensive, and preferential insertion of members of the miniature inverted-repeat transposable element family Heartbreaker into genic regions of maize. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[4]  B. Charlesworth,et al.  Fixation of transposable elements in the Drosophila melanogaster genome. , 2005, Genetical research.

[5]  D. Petrov,et al.  High intrinsic rate of DNA loss in Drosophila , 1996, Nature.

[6]  C. Langley,et al.  Chromosome rearrangement by ectopic recombination in Drosophila melanogaster: genome structure and evolution. , 1991, Genetics.

[7]  J. Bennetzen,et al.  Mechanisms of recent genome size variation in flowering plants. , 2005, Annals of botany.

[8]  M. Morgante,et al.  Gene duplication and exon shuffling by helitron-like transposons generate intraspecies diversity in maize , 2005, Nature Genetics.

[9]  Mattias Jakobsson,et al.  The Pattern of Polymorphism in Arabidopsis thaliana , 2005, PLoS biology.

[10]  S. Wessler,et al.  Dramatic amplification of a rice transposable element during recent domestication , 2006, Proceedings of the National Academy of Sciences.

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

[12]  Takuji Sasaki,et al.  The map-based sequence of the rice genome , 2005, Nature.

[13]  Brian Charlesworth,et al.  On the abundance and distribution of transposable elements in the genome of Drosophila melanogaster. , 2002, Molecular biology and evolution.

[14]  A. E. Hirsh,et al.  Size matters: non-LTR retrotransposable elements and ectopic recombination in Drosophila. , 2003, Molecular biology and evolution.

[15]  James K. M. Brown,et al.  Genome size reduction through illegitimate recombination counteracts genome expansion in Arabidopsis. , 2002, Genome research.

[16]  S. Wessler,et al.  Treasures in the attic: Rolling circle transposons discovered in eukaryotic genomes , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Joachim Messing,et al.  Gene movement by Helitron transposons contributes to the haplotype variability of maize. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[18]  J. Jurka,et al.  Rolling-circle transposons in eukaryotes , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[19]  B. Charlesworth,et al.  The distribution of transposable elements within and between chromosomes in a population of Drosophila melanogaster. II. Inferences on the nature of selection against elements. , 1992, Genetical research.

[20]  M. G. Kidwell,et al.  Transposable elements and the evolution of genome size in eukaryotes , 2002, Genetica.

[21]  C. Hoogland,et al.  Chromosomal distribution of transposable elements in Drosophila melanogaster: test of the ectopic recombination model for maintenance of insertion site number. , 1996, Genetics.

[22]  S. Wright,et al.  Effects of recombination rate and gene density on transposable element distributions in Arabidopsis thaliana. , 2003, Genome research.

[23]  O. Panaud,et al.  Formation of solo-LTRs through unequal homologous recombination counterbalances amplifications of LTR retrotransposons in rice Oryza sativa L. , 2003, Molecular biology and evolution.

[24]  Sudhir Kumar,et al.  MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment , 2004, Briefings Bioinform..

[25]  B. Gaut,et al.  Transcription-related mutations and GC content drive variation in nucleotide substitution rates across the genomes of Arabidopsis thaliana and Arabidopsis lyrata , 2007, BMC Evolutionary Biology.

[26]  S. Nuzhdin Sure facts, speculations, and open questions about the evolution of transposable element copy number , 2004, Genetica.

[27]  P. Schulze-Lefert,et al.  A contiguous 66-kb barley DNA sequence provides evidence for reversible genome expansion. , 2000, Genome research.

[28]  B. Charlesworth,et al.  A test for the role of natural selection in the stabilization of transposable element copy number in a population of Drosophila melanogaster. , 1987, Genetical research.

[29]  G. Gloor,et al.  Homology requirements for targeting heterologous sequences during P-induced gap repair in Drosophila melanogaster. , 1997, Genetics.

[30]  Giorgio Pea,et al.  Origins, genetic organization and transcription of a family of non-autonomous helitron elements in maize. , 2005, The Plant journal : for cell and molecular biology.

[31]  J. Bennetzen,et al.  Transposable elements, gene creation and genome rearrangement in flowering plants. , 2005, Current opinion in genetics & development.

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

[33]  Shelby L. Bidwell,et al.  A potentially functional mariner transposable element in the protist Trichomonas vaginalis. , 2004, Molecular biology and evolution.

[34]  J. Dvorak,et al.  Recombination: an underappreciated factor in the evolution of plant genomes , 2007, Nature Reviews Genetics.

[35]  S. Wright,et al.  Population dynamics of an Ac-like transposable element in self- and cross-pollinating arabidopsis. , 2001, Genetics.

[36]  T. Eickbush,et al.  Retrotransposable elements R1 and R2 interrupt the rRNA genes of most insects. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[37]  T. A. Hall,et al.  BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT , 1999 .