Local chromosome context is a major determinant of crossover pathway biochemistry during budding yeast meiosis

  1. Darpan Medhi
  2. Alastair SH Goldman
  3. Michael Lichten  Is a corresponding author
  1. National Cancer Institute, United States
  2. The University of Sheffield, United Kingdom

Abstract

The budding yeast genome contains regions where meiotic recombination initiates more frequently than in others. This pattern parallels enrichment for the meiotic chromosome axis proteins Hop1 and Red1. These proteins are important for Spo11-catalyzed double strand break formation; their contribution to crossover recombination remains undefined. Using the sequence-specific VMA1-derived endonuclease (VDE) to initiate recombination in meiosis, we show that chromosome structure influences the choice of proteins that resolve recombination intermediates to form crossovers. At a Hop1-enriched locus, most VDE-initiated crossovers, like most Spo11-initiated crossovers, required the meiosis-specific MutLγ resolvase. In contrast, at a locus with lower Hop1 occupancy, most VDE-initiated crossovers were MutLγ-independent. In pch2 mutants, the two loci displayed similar Hop1 occupancy levels, and VDE-induced crossovers were similarly MutLγ-dependent. We suggest that meiotic and mitotic recombination pathways coexist within meiotic cells, and that features of meiotic chromosome structure determine whether one or the other predominates in different regions.

Article and author information

Author details

  1. Darpan Medhi

    Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, United States
    Competing interests
    The authors declare that no competing interests exist.
  2. Alastair SH Goldman

    Sheffield Institute for Nucleic Acids, The University of Sheffield, Sheffield, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  3. Michael Lichten

    Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, United States
    For correspondence
    mlichten@helix.nih.gov
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-9707-2956

Funding

Intramural Research Program of the NIH through the Center for Cancer Research at the National Cancer Institute (Intramural research award)

  • Michael Lichten

University of Sheffield (Graduate tuition grant)

  • Darpan Medhi

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

Metrics

  • 1,793
    views
  • 529
    downloads
  • 30
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Citations by DOI

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Darpan Medhi
  2. Alastair SH Goldman
  3. Michael Lichten
(2016)
Local chromosome context is a major determinant of crossover pathway biochemistry during budding yeast meiosis
eLife 5:e19669.
https://doi.org/10.7554/eLife.19669

Share this article

https://doi.org/10.7554/eLife.19669