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Article
Nature 454, 479-485 (24 July 2008) | doi:10.1038/nature07135; Received 10 March 2008; Accepted 30 May 2008; Published online 9 July 2008
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Postdoctoral Position (CNS Biomarkers)
- F. Hoffmann-La Roche AG
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- Nature Publishing Group
- New York, NY
High-resolution mapping of meiotic crossovers and non-crossovers in yeast
Eugenio Mancera1,3, Richard Bourgon2,3, Alessandro Brozzi2, Wolfgang Huber2 & Lars M. Steinmetz1
- European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany
- European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge CB10 1SD, UK
- These authors contributed equally to this work.
Correspondence to: Lars M. Steinmetz1 Correspondence and requests for materials should be addressed to L.M.S. (Email: larsms@embl.de).
Abstract
Meiotic recombination has a central role in the evolution of sexually reproducing organisms. The two recombination outcomes, crossover and non-crossover, increase genetic diversity, but have the potential to homogenize alleles by gene conversion. Whereas crossover rates vary considerably across the genome, non-crossovers and gene conversions have only been identified in a handful of loci. To examine recombination genome wide and at high spatial resolution, we generated maps of crossovers, crossover-associated gene conversion and non-crossover gene conversion using dense genetic marker data collected from all four products of fifty-six yeast (Saccharomyces cerevisiae) meioses. Our maps reveal differences in the distributions of crossovers and non-crossovers, showing more regions where either crossovers or non-crossovers are favoured than expected by chance. Furthermore, we detect evidence for interference between crossovers and non-crossovers, a phenomenon previously only known to occur between crossovers. Up to 1% of the genome of each meiotic product is subject to gene conversion in a single meiosis, with detectable bias towards GC nucleotides. To our knowledge the maps represent the first high-resolution, genome-wide characterization of the multiple outcomes of recombination in any organism. In addition, because non-crossover hotspots create holes of reduced linkage within haplotype blocks, our results stress the need to incorporate non-crossovers into genetic linkage analysis.
- European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany
- European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge CB10 1SD, UK
- These authors contributed equally to this work.
Correspondence to: Lars M. Steinmetz1 Correspondence and requests for materials should be addressed to L.M.S. (Email: larsms@embl.de).
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