Evidence map›Paper›PMID 29084572›Full record

ArticleGenome biology2017

Meiotic crossovers are associated with open chromatin and enriched with Stowaway transposons in potato.

Alexandre P Marand, Shelley H Jansky, Hainan Zhao, Courtney P Leisner, Xiaobiao Zhu, Zixian Zeng, Emily Crisovan, Linsey Newton, Andy J Hamernik, Richard E Veilleux and 2 more

Abstract read
In one paragraph

Article in Genome biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed.

  1. On the origin of PRDM9-guided recombination hotspots.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  9. The Quest for thePotato research · 2025
    Article
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  13. High prevalence of PRDM9-independent recombination hotspots in placental mammals.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Molecular mechanisms and regulation of recombination frequency and distribution in plants.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Review
  15. Article
  16. Epigenetic regulation during meiosis and crossover.Physiology and molecular biology of plants : an international journal of functional plant biology · 2023
    Review
  17. Article
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  20. Crossover patterning in plants.Plant reproduction · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Alexandre P MarandDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA.
Shelley H JanskyDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA. shjansky@wisc.edu.
Hainan ZhaoDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA.
Courtney P LeisnerDepartment of Plant Biology, Michigan State University, East Lansing, Michigan, 48824, USA.
Xiaobiao ZhuDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA.
Zixian ZengDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA.
Emily CrisovanDepartment of Plant Biology, Michigan State University, East Lansing, Michigan, 48824, USA.
Linsey NewtonDepartment of Plant Biology, Michigan State University, East Lansing, Michigan, 48824, USA.
Andy J HamernikDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA.
Richard E VeilleuxDepartment of Horticulture, Virginia Tech, Blacksburg, VA, 24061, USA.
C Robin BuellDepartment of Plant Biology, Michigan State University, East Lansing, Michigan, 48824, USA.
Jiming JiangDepartment of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin, 53706, USA. jiangjm@msu.edu.ORCID 0000-0002-6435-6140

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMeiotic recombination is the foundation for genetic variation in natural and artificial populations of eukaryotes. Although genetic maps have been developed for numerous plant species since the late 1980s, few of these maps have provided the necessary resolution needed to investigate the genomic and epigenomic features underlying meiotic crossovers.

resultsUsing a whole genome sequencing-based approach, we developed two high-density reference-based haplotype maps using diploid potato clones as parents. The vast majority (81%) of meiotic crossovers were mapped to less than 5 kb. The fine-scale accuracy of crossover detection was validated by Sanger sequencing for a subset of ten crossover events. We demonstrate that crossovers reside in genomic regions of "open chromatin", which were identified based on hypersensitivity to DNase I digestion and association with H3K4me3-modified nucleosomes. The genomic regions spanning crossovers were significantly enriched with the Stowaway family of miniature inverted-repeat transposable elements (MITEs). The occupancy of Stowaway elements in gene promoters is concomitant with an increase in recombination rate. A generalized linear model identified the presence of Stowaway elements as the third most important genomic or chromatin feature behind genes and open chromatin for predicting crossover formation over 10-kb windows.

conclusionsCollectively, our results suggest that meiotic crossovers in potato are largely determined by the local chromatin status, marked by accessible chromatin, H3K4me3-modified nucleosomes, and the presence of Stowaway transposons.

Indexed as

Crossing Over, GeneticDNA Transposable ElementsChromatinChromosome MappingChromosomes, PlantGenomicsHaplotypesMeiosisSolanum tuberosumChromatinDNA Transposable Elements

Identifiers

PMID29084572
PMCPMC5663088

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.