Origin and evolution of new exons in rodents

  1. Wen Wang1,9,10,
  2. Hongkun Zheng2,9,
  3. Shuang Yang1,3,9,
  4. Haijing Yu4,9,
  5. Jun Li2,
  6. Huifeng Jiang1,3,
  7. Jianning Su2,
  8. Lei Yang2,
  9. Jianguo Zhang2,
  10. Jason McDermott5,
  11. Ram Samudrala5,
  12. Jian Wang2,
  13. Huanming Yang2,
  14. Jun Yu2,
  15. Karsten Kristiansen8,
  16. Gane Ka-Shu Wong2,6,10, and
  17. Jun Wang2,7,8,10
  1. 1 CAS-Max Planck Junior Research Group, Key Laboratory of Cellular and Molecular Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China
  2. 2 Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 101300, China
  3. 3 Graduate School of Chinese Academy Sciences, Beijing 100039, China
  4. 4 Key Laboratory of Biodiversity Conservation and Utilization & Human Genetics Center of Yunnan University, Kunming, Yunnan 650091, China
  5. 5 Computational Genomics Group, Department of Microbiology, University of Washington, Seattle, Washington 98195, USA
  6. 6 UW Genome Center, Department of Medicine, University of Washington, Seattle, Washington 98195, USA
  7. 7 The Institute of Human Genetics, University of Aarhus, DK-8000 Aarhus C, Denmark
  8. 8 Department of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense M, Denmark

Abstract

Gene number difference among organisms demonstrates that new gene origination is a fundamental biological process in evolution. Exon shuffling has been universally observed in the formation of new genes. Yet to be learned are the ways new exons originate and evolve, and how often new exons appear. To address these questions, we identified 2695 newly evolved exons in the mouse and rat by comparing the expressed sequences of 12,419 orthologous genes between human and mouse, using 743,856 pig ESTs as the outgroup. The new exon origination rate is about 2.71 × 10-3 per gene per million years. These new exons have markedly accelerated rates both of nonsynonymous substitutions and of insertions/deletions (indels). A much higher proportion of new exons have Ka/Ks ratios >1 (where Ka is the nonsynonymous substitution rate and Ks is the synonymous substitution rate) than do the old exons shared by human and mouse, implying a role of positive selection in the rapid evolution. The majority of these new exons have sequences unique in the genome, suggesting that most new exons might originate through “exonization” of intronic sequences. Most of the new exons appear to be alternative exons that are expressed at low levels.

Footnotes

  • [Supplemental material is available online at www.genome.org.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.3929705. Article published online before print in August 2005.

  • 9 These authors contributed equally to this work.

  • 10 Corresponding authors. E-mail wwang{at}mail.kiz.ac.cn; fax 86-871-5193137. E-mail gksw{at}genomics.org.cn; fax 86-10-80498676. E-mail wangj{at}genomics.org.cn; fax 86-10-80498676.

    • Accepted June 14, 2005.
    • Received December 28, 2004.
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