Human, Mouse, and Rat Genome Large-Scale Rearrangements: Stability Versus Speciation

  1. Shaying Zhao1,3,
  2. Jyoti Shetty1,
  3. Lihua Hou1,
  4. Arthur Delcher1,
  5. Baoli Zhu2,
  6. Kazutoyo Osoegawa2,
  7. Pieter de Jong2,
  8. William C. Nierman1,
  9. Robert L. Strausberg1, and
  10. Claire M. Fraser1
  1. 1The Institute for Genomic Research, Rockville, Maryland 20850, USA
  2. 2BACPAC Resources, Children's Hospital Oakland Research Institute, Oakland, California 94609, USA

Abstract

Using paired-end sequences from bacterial artificial chromosomes, we have constructed high-resolution synteny and rearrangement breakpoint maps among human, mouse, and rat genomes. Among the >300 syntenic blocks identified are segments of over 40 Mb without any detected interspecies rearrangements, as well as regions with frequently broken synteny and extensive rearrangements. As closely related species, mouse and rat share the majority of the breakpoints and often have the same types of rearrangements when compared with the human genome. However, the breakpoints not shared between them indicate that mouse rearrangements are more often interchromosomal, whereas intrachromosomal rearrangements are more prominent in rat. Centromeres may have played a significant role in reorganizing a number of chromosomes in all three species. The comparison of the three species indicates that genome rearrangements follow a path that accommodates a delicate balance between maintaining a basic structure underlying all mammalian species and permitting variations that are necessary for speciation.

Footnotes

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

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.2663304. Article published online before print in September 2004.

  • 3 Corresponding author. E-MAIL szhao{at}tigr.org; FAX (301) 838-0208.

    • Accepted August 11, 2004.
    • Received April 8, 2004.
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