New Evidence for Genome-Wide Duplications at the Origin of Vertebrates Using an Amphioxus Gene Set and Completed Animal Genomes

  1. Georgia Panopoulou1,4,
  2. Steffen Hennig2,
  3. Detlef Groth2,
  4. Antje Krause3,
  5. Albert J. Poustka1,
  6. Ralf Herwig2,
  7. Martin Vingron3, and
  8. Hans Lehrach1,2
  1. 1 Evolution and Development Group, Department Professor H. Lehrach, Max-Planck Institut für Molekulare Genetik, D-14195 Berlin, Germany
  2. 2 Bioinformatics Group, Department Professor H. Lehrach, Max-Planck Institut für Molekulare Genetik, D-14195 Berlin, Germany
  3. 3 Computational Molecular Biology, Department Professor M. Vingron, Max-Planck Institut für Molekulare Genetik, D-14195 Berlin, Germany

Abstract

The 2R hypothesis predicting two genome duplications at the origin of vertebrates is highly controversial. Studies published so far include limited sequence data from organisms close to the hypothesized genome duplications. Through the comparison of a gene catalog from amphioxus, the closest living invertebrate relative of vertebrates, to 3453 single-copy genes orthologous between Caenorhabditis elegans (C), Drosophila melanogaster (D), and Saccharomyces cerevisiae (Y), and to Ciona intestinalis ESTs, mouse, and human genes, we show with a large number of genes that the gene duplication activity is significantly higher after the separation of amphioxus and the vertebrate lineages, which we estimate at 650 million years (Myr). The majority of human orthologs of 195 CDY groups that could be dated by the molecular clock appear to be duplicated between 300 and 680 Myr with a mean at 488 million years ago (Mya). We detected 485 duplicated chromosomal segments in the human genome containing CDY orthologs, 331 of which are found duplicated in the mouse genome and within regions syntenic between human and mouse, indicating that these were generated earlier than the human–mouse split. Model based calculations of the codon substitution rate of the human genes included in these segments agree with the molecular clock duplication time-scale prediction. Our results favor at least one large duplication event at the origin of vertebrates, followed by smaller scale duplication closer to the bird–mammalian split.

Footnotes

  • [Supplementary material is available online at www.genome.org. The cDNA clones used in the EST sequencing are available from http://www.rzpd.de/. All ESTs are deposited in dbEST (accession nos. BI385298–BI388632, BI378370–BI381823, BI381824–BI385297, and BI376198–BI378369). The consensus of the alignments of the C, D, Y, orthologs included in the CD/CDY groups that we describe are available for similarity searches at http://www.molgen.mpg.de/~amphioxus.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.874803.

  • 4 Corresponding author. E-MAIL panopoul{at}molgen.mpg.de; FAX 49-30-84131128.

    • Accepted March 24, 2003.
    • Received October 7, 2002.
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