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PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice

Source: Science 327, 836 (2010); doi:10.1126/science.1183439

Published December 31, 2009

PUBLICATION DATA
ISSN:
1553-9628 (online)
Publisher:
AIP is a member of CrossRef AAAS
F. Baudat,ff1 J. Buard,ff1 C. Grey,ff1 A. Fledel-Alon,ff2 C. Ober,ff2 M. Przeworski,ff2,ff3 G. Coop,ff4 and B. de Massyff1
ff1Institut de Gntique Humaine, UPR1142, CNRS, Montpellier, France.
ff2Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
ff3Howard Hughes Medical Institute, University of Chicago, Chicago, IL 60637, USA.
ff4Department of Evolution and Ecology and the Center for Population Biology, University of California, Davis, CA 95616, USA.

Meiotic recombination events cluster into narrow segments of the genome, defined as hotspots. Here, we demonstrate that a major player for hotspot specification is the Prdm9 gene. First, two mouse strains that differ in hotspot usage are polymorphic for the zinc finger DNA binding array of PRDM9. Second, the human consensus PRDM9 allele is predicted to recognize the 13-mer motif enriched at human hotspots; this DNA binding specificity is verified by in vitro studies. Third, allelic variants of PRDM9 zinc fingers are significantly associated with variability in genome-wide hotspot usage among humans. Our results provide a molecular basis for the distribution of meiotic recombination in mammals, in which the binding of PRDM9 to specific DNA sequences targets the initiation of recombination at specific locations in the genome. ©2010 American Association for the Advancement of Science

(As supplied by publisher.)

History: Received October 16, 2009; accepted December 17, 2009; published December 31, 2009
Permalink: http://dx.doi.org/10.1126/science.1183439
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