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Published online before print December 12, 2005, 10.1101/gr.3810906
Genome Res. 16:88-96, 2006
©2006 by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/06 $5.00
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Letter

The evolutionary dynamics of {alpha}-satellite

M. Katharine Rudd1,2,4, Gregory A. Wray1,3 and Huntington F. Willard1,2,3,5

1 Institute for Genome Sciences & Policy, Duke University, Durham, North Carolina 27708, USA 2 Department of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina 27708, USA 3 Department of Biology, Duke University, Durham, North Carolina 27708, USA

{alpha}-Satellite is a family of tandemly repeated sequences found at all normal human centromeres. In addition to its significance for understanding centromere function, {alpha}-satellite is also a model for concerted evolution, as {alpha}-satellite repeats are more similar within a species than between species. There are two types of {alpha}-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 {alpha}-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 {alpha}-satellite in the human genome assembly. Monomeric and higher-order {alpha}-satellites on chromosome 17 are phylogenetically distinct, consistent with a model in which higher-order evolved independently of monomeric {alpha}-satellite. Comparative analysis between human chromosome 17 and the orthologous chimpanzee chromosome indicates that monomeric {alpha}-satellite is evolving at approximately the same rate as the adjacent non-{alpha}-satellite DNA. However, higher-order {alpha}-satellite is less conserved, suggesting different evolutionary rates for the two types of {alpha}-satellite.


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.

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


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