Natural variation and dosage of the HEI10 meiotic E3 ligase control Arabidopsis crossover recombination

  1. Ian R. Henderson1
  1. 1Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom;
  2. 2Department of Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland;
  3. 3Howard Hughes Medical Institute, Gordon and Betty Moore Foundation, Watson School of Biological Sciences, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA;
  4. 4School of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom
  1. Corresponding author: irh25{at}cam.ac.uk
  1. 5 These authors contributed equally to this work.

Abstract

During meiosis, homologous chromosomes undergo crossover recombination, which creates genetic diversity and balances homolog segregation. Despite these critical functions, crossover frequency varies extensively within and between species. Although natural crossover recombination modifier loci have been detected in plants, causal genes have remained elusive. Using natural Arabidopsis thaliana accessions, we identified two major recombination quantitative trait loci (rQTLs) that explain 56.9% of crossover variation in Col×Ler F2 populations. We mapped rQTL1 to semidominant polymorphisms in HEI10, which encodes a conserved ubiquitin E3 ligase that regulates crossovers. Null hei10 mutants are haploinsufficient, and, using genome-wide mapping and immunocytology, we show that transformation of additional HEI10 copies is sufficient to more than double euchromatic crossovers. However, heterochromatic centromeres remained recombination-suppressed. The strongest HEI10-mediated crossover increases occur in subtelomeric euchromatin, which is reminiscent of sex differences in Arabidopsis recombination. Our work reveals that HEI10 naturally limits Arabidopsis crossovers and has the potential to influence the response to selection.

Keywords

Footnotes

  • Supplemental material is available for this article.

  • Article published online ahead of print. Article and publication date are online at http://www.genesdev.org/cgi/doi/10.1101/gad.295501.116.

  • Freely available online through the Genes & Development Open Access option.

  • Received December 22, 2016.
  • Accepted January 27, 2017.

This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.

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