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Genetics. 2019 Nov;213(3):771-787. doi: 10.1534/genetics.119.302406. Epub 2019 Sep 16.

An Ultra High-Density Arabidopsis thaliana Crossover Map That Refines the Influences of Structural Variation and Epigenetic Features.

Author information

1
Department of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany browan@ucdavis.edu.
2
Earlham Institute, Norwich NR4 7UZ, United Kingdom.
3
Department of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany.
4
Department of Plant Sciences, University of Cambridge, CB2 3EA, United Kingdom.

Abstract

Many environmental, genetic, and epigenetic factors are known to affect the frequency and positioning of meiotic crossovers (COs). Suppression of COs by large, cytologically visible inversions and translocations has long been recognized, but relatively little is known about how smaller structural variants (SVs) affect COs. To examine fine-scale determinants of the CO landscape, including SVs, we used a rapid, cost-effective method for high-throughput sequencing to generate a precise map of >17,000 COs between the Col-0 and Ler-0 accessions of Arabidopsis thaliana COs were generally suppressed in regions with SVs, but this effect did not depend on the size of the variant region, and was only marginally affected by the variant type. CO suppression did not extend far beyond the SV borders and CO rates were slightly elevated in the flanking regions. Disease resistance gene clusters, which often exist as SVs, exhibited high CO rates at some loci, but there was a tendency toward depressed CO rates at loci where large structural differences exist between the two parents. Our high-density map also revealed in fine detail how CO positioning relates to genetic (DNA motifs) and epigenetic (chromatin structure) features of the genome. We conclude that suppression of COs occurs over a narrow region spanning large- and small-scale SVs, representing an influence on the CO landscape in addition to sequence and epigenetic variation along chromosomes.

KEYWORDS:

double-strand break; genetic map; meiosis; recombination; structural variation

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