The evolutionary dynamics of α-satellite

  1. M. Katharine Rudd1,2,4,
  2. Gregory A. Wray1,3, and
  3. Huntington F. Willard1,2,3,5
  1. 1 Institute for Genome Sciences & Policy, Duke University, Durham, North Carolina 27708, USA
  2. 2 Department of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina 27708, USA
  3. 3 Department of Biology, Duke University, Durham, North Carolina 27708, USA

Abstract

α-Satellite is a family of tandemly repeated sequences found at all normal human centromeres. In addition to its significance for understanding centromere function, α-satellite is also a model for concerted evolution, as α-satellite repeats are more similar within a species than between species. There are two types of α-satellite in the human genome; while both are made up of ∼171-bp monomers, they can be distinguished by whether monomers are arranged in extremely homogeneous higher-order, multimeric repeat units or exist as more divergent monomeric α-satellite that lacks any multimeric periodicity. In this study, as a model to examine the genomic and evolutionary relationships between these two types, we have focused on the chromosome 17 centromeric region that has reached both higher-order and monomeric α-satellite in the human genome assembly. Monomeric and higher-order α-satellites on chromosome 17 are phylogenetically distinct, consistent with a model in which higher-order evolved independently of monomeric α-satellite. Comparative analysis between human chromosome 17 and the orthologous chimpanzee chromosome indicates that monomeric α-satellite is evolving at approximately the same rate as the adjacent non-α-satellite DNA. However, higher-order α-satellite is less conserved, suggesting different evolutionary rates for the two types of α-satellite.

Footnotes

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

  • Article published online ahead of print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.3810906.

  • 4 Present address: Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

  • 5 Corresponding author. E-mail hunt.willard{at}duke.edu; fax (919) 668-0795.

    • Accepted September 12, 2005.
    • Received February 8, 2005.
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