An Active Non-LTR Retrotransposon With Tandem Structure in the Compact Genome of the Pufferfish Tetraodon nigroviridis

  1. Laurence Bouneau1,4,
  2. Cécile Fischer1,4,
  3. Catherine Ozouf-Costaz2,
  4. Alexander Froschauer3,
  5. Olivier Jaillon1,
  6. Jean-Pierre Coutanceau2,
  7. Cornelia Körting3,
  8. Jean Weissenbach1,
  9. Alain Bernot1, and
  10. Jean-Nicolas Volff3,5
  1. 1 Genoscope/Centre National de Séquençage and CNRS-UMR 8030, F-91057 Evry Cedex 06, France
  2. 2 Laboratoire d'Ichtyologie and Service de Systématique Moléculaire, CNRS IFR 1541, Muséum National d'Histoire Naturelle, F-75231 Paris Cedex 05, France
  3. 3 BioFuture Research Group “Evolutionary Fish Genomics”, Physiologische Chemie I, Biozentrum, University of Würzburg, D-97074 Würzburg, Germany

Abstract

The fish retrotransposable element Zebulon encodes a reverse transcriptase and a carboxy-terminal restriction enzyme-like endonuclease, and is related phylogenetically to site-specific non-LTR retrotransposons from nematodes. Zebulon was detected in the pufferfishes Tetraodon nigroviridis and Takifugu rubripes, as well as in the zebrafish Danio rerio. Structural analysis suggested that Zebulon, in contrast to most non-LTR retrotransposons, might be able to retrotranspose as a partial tandem array. Zebulon was active relatively recently in the compact genome of T. nigroviridis, in which it contributed to the extension of intergenic and intronic sequences, and possibly to the formation of genomic rearrangements. Accumulation of Zebulon together with other retrotransposons was observed in some heterochromatic chromosomal regions of the genome of T. nigroviridis that might serve as reservoirs for active elements. Hence, pufferfish compact genomes are not evolutionarily inert and contain active retrotransposons, suggesting the presence of mechanisms allowing accumulation of retrotransposable elements in heterochromatin, but minimizing their impact on euchromatic regions. Homologous recombination between partial tandem sequences eliminating active copies of Zebulon and reducing the size of insertions in intronic and intragenic regions might represent such a mechanism.

Footnotes

  • Article published online before print in June 2003.

    [The sequence data from this study have been submitted to GenBank/EMBL under accession nos. AL808032, AY135221, AJ496734, AJ496221, AJ496222, AJ496223, AJ496224, and AJ496225.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.726003.

  • 4 These authors contributed equally to this work.

  • 5 Corresponding author. E-MAIL volff{at}biozentrum.uni-wuerzburg.de; FAX (0) 931-888-4150.

    • Accepted April 18, 2003.
    • Received August 21, 2002.
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