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Genetics. 2017 Jun;206(2):603-619. doi: 10.1534/genetics.116.197988.

Structural Variation Shapes the Landscape of Recombination in Mouse.

Author information

1
Department of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599-7264.
2
The Jackson Laboratory, Bar Harbor, Maine 04609.
3
Department of Computer Science, University of North Carolina, Chapel Hill, North Carolina 27599-7264.
4
European Bioinformatics Institute, Hinxton, Cambridge, CB10 1SD, United Kingdom.
5
Center for Sleep and Circadian Neurobiology, University of Pennsylvania, Philadelphia, Pennsylvania 19104-3403.
6
UCL Genetics Institute, University College London, WC1E 6BT, United Kingdom.
7
The Jackson Laboratory, Bar Harbor, Maine 04609 fernando@med.unc.edu gary.churchill@jax.org.
8
Department of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599-7264 fernando@med.unc.edu gary.churchill@jax.org.

Abstract

Meiotic recombination is an essential feature of sexual reproduction that ensures faithful segregation of chromosomes and redistributes genetic variants in populations. Multiparent populations such as the Diversity Outbred (DO) mouse stock accumulate large numbers of crossover (CO) events between founder haplotypes, and thus present a unique opportunity to study the role of genetic variation in shaping the recombination landscape. We obtained high-density genotype data from [Formula: see text] DO mice, and localized 2.2 million CO events to intervals with a median size of 28 kb. The resulting sex-averaged genetic map of the DO population is highly concordant with large-scale (order 10 Mb) features of previously reported genetic maps for mouse. To examine fine-scale (order 10 kb) patterns of recombination in the DO, we overlaid putative recombination hotspots onto our CO intervals. We found that CO intervals are enriched in hotspots compared to the genomic background. However, as many as [Formula: see text] of CO intervals do not overlap any putative hotspots, suggesting that our understanding of hotspots is incomplete. We also identified coldspots encompassing 329 Mb, or [Formula: see text] of observable genome, in which there is little or no recombination. In contrast to hotspots, which are a few kilobases in size, and widely scattered throughout the genome, coldspots have a median size of 2.1 Mb and are spatially clustered. Coldspots are strongly associated with copy-number variant (CNV) regions, especially multi-allelic clusters, identified from whole-genome sequencing of 228 DO mice. Genes in these regions have reduced expression, and epigenetic features of closed chromatin in male germ cells, which suggests that CNVs may repress recombination by altering chromatin structure in meiosis. Our findings demonstrate how multiparent populations, by bridging the gap between large-scale and fine-scale genetic mapping, can reveal new features of the recombination landscape.

KEYWORDS:

MPP; copy-number variation; genetic mapping; meiotic recombination; multiparental populations; recombination hotspots

PMID:
28592499
PMCID:
PMC5499175
DOI:
10.1534/genetics.116.197988
[Indexed for MEDLINE]
Free PMC Article

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