Medical Journals

Comparison of Multiple Vertebrate Genomes Reveals the Birth and Evolution of Human Exons.

Authors:
  • Zhang Xiang H-F
  • Chasin Lawrence A

From: Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

Proceedings of the National Academy of Sciences of the United States of America

  • Publish Date: Sep 2006
  • ISSN: 0027-8424
  • Volume: 103
  • Issue: 36
  • Pages: 13427-32
  • Medium: Print
  • Language: English
  • Citation (JAMA): Zhang Xiang H-F, Chasin Lawrence A, et al. Comparison of Multiple Vertebrate Genomes Reveals the Birth and Evolution of Human Exons.. Proc. Natl. Acad. Sci. U.S.A. Sep 2006;103:13427-32

Abstract

Orthologous gene structures in eight vertebrate species were compared on a genomic scale to detect the birth and maturation of new internal exons during the course of evolution. We found that 40% of new human exons are alternatively spliced, and most of these are cassette exons (exons that are either included or skipped in their entirety) with low inclusion rates. This proportion decreases steadily as older and older exons are examined, even as splicing efficiency increases. Remarkably, the great majority of new cassette exons are composed of highly repeated sequences, especially Alu. Many new cassette exons are 5’ untranslated exons; the proportion that code for protein increases steadily with age. New protein-coding exons evolve at a high rate, as evidenced by the initially high substitution rates (K(s) and K(a)), as well as the SNP density compared with older exons. This dynamic picture suggests that de novo recruitment rather than shuffling is the major route by which exons are added to genes, and that species-specific repeats could play a significant role in recent evolution.

Mesh Headings (Keywords): Alternative Splicing, Alu Elements, Animals, Evolution, Molecular, Exons, Expressed Sequence Tags, Gene Expression Profiling, Genome, Humans, Kinetics, Polymorphism, Single Nucleotide, Species Specificity, Tandem Repeat Sequences, Tissue Distribution, Transcription, Genetic, Vertebrates


Check for Full Text / PubMed Unique Identifier (PMID): 16938881


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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