A comprehensive molecular cytogenetic analysis of chromosome rearrangements in gibbons

  1. Nicoletta Archidiacono1,8
  1. 1Department of Genetics and Microbiology, University of Bari, 70126 Bari, Italy;
  2. 2Children's Hospital of Oakland Research Institute, Oakland, California 94609, USA;
  3. 3Department of Evolutionary Biology, University of Florence, 50125 Florence, Italy;
  4. 4The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101SA, United Kingdom;
  5. 5Center for Spoken Language Understanding, Oregon Health & Science University (OHSU), Portland, Oregon 97239, USA
    1. 6 These authors contributed equally to this work.

    • 7 Present address: Oregon Health & Science University (OHSU), Portland, Oregon 97239, USA.

    Abstract

    Chromosome rearrangements in small apes are up to 20 times more frequent than in most mammals. Because of their complexity, the full extent of chromosome evolution in these hominoids is not yet fully documented. However, previous work with array painting, BAC-FISH, and selective sequencing in two of the four karyomorphs has shown that high-resolution methods can precisely define chromosome breakpoints and map the complex flow of evolutionary chromosome rearrangements. Here we use these tools to precisely define the rearrangements that have occurred in the remaining two karyomorphs, genera Symphalangus (2n = 50) and Hoolock (2n = 38). This research provides the most comprehensive insight into the evolutionary origins of chromosome rearrangements involved in transforming small apes genome. Bioinformatics analyses of the human–gibbon synteny breakpoints revealed association with transposable elements and segmental duplications, providing some insight into the mechanisms that might have promoted rearrangements in small apes. In the near future, the comparison of gibbon genome sequences will provide novel insights to test hypotheses concerning the mechanisms of chromosome evolution. The precise definition of synteny block boundaries and orientation, chromosomal fusions, and centromere repositioning events presented here will facilitate genome sequence assembly for these close relatives of humans.

    Footnotes

    • 8 Corresponding author

      E-mail archidiacono{at}biologia.uniba.it

    • [Supplemental material is available for this article.]

    • Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.138651.112.

    • Received February 5, 2012.
    • Accepted August 13, 2012.

    This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.

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