Evidence map›Paper›PMID 30903284›Full record

ArticlePlant reproduction2019

Transgenerational effects of inter-ploidy cross direction on reproduction and F2 seed development of Arabidopsis thaliana F1 hybrid triploids.

Dorota Duszynska, Bjarni Vilhjalmsson, Rosa Castillo Bravo, Sandesh Swamidatta, Thomas E Juenger, Mark T A Donoghue, Aurélie Comte, Magnus Nordborg, Timothy F Sharbel, Galina Brychkova and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Plant reproduction, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Triploid cultivars ofFrontiers in plant science · 2022
    Article
  5. Article
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 at 5 institutions in 7 countries.

Dorota DuszynskaGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.
Bjarni VilhjalmssonGregor Mendel Institute of Molecular Plant Biology, Vienna, Austria.ORCID 0000-0003-2277-9249
Rosa Castillo BravoGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.
Sandesh SwamidattaGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.
Thomas E JuengerSection of Integrative Biology and Institute for Cellular and Molecular Biology, University of Texas, Austin, USA.ORCID 0000-0001-9550-9288
Mark T A DonoghueGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.
Aurélie ComteGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.
Magnus NordborgGregor Mendel Institute of Molecular Plant Biology, Vienna, Austria.ORCID 0000-0001-7178-9748
Timothy F SharbelApomixis Research Group, Department of Cytogenetics and Genome Analysis, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Gatersleben, Germany.ORCID 0000-0002-3450-2733
Galina BrychkovaGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.
Peter C McKeownGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland.ORCID 0000-0002-7255-6062
Charles SpillaneGenetics and Biotechnology Laboratory, Plant and AgriBiosciences Research Centre (PABC), Ryan Institute, National University of Ireland, Galway, H91 REW4, Ireland. charles.spillane@nuigalway.ie.ORCID 0000-0003-3318-323X
Ollscoil na Gaillimhe – University of Galway · IEGregor Mendel Institute of Molecular Plant Biology · ATLeibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK) · DEMemorial Sloan Kettering Cancer Center · USThe University of Texas at Austin · US

Funding

Science Foundation Ireland 02/IN.1/B49Science Foundation Ireland 08/IN.1/B1931
6 · The paper itself

Abstract

key messageReproduction in triploid plants is important for understanding polyploid population dynamics. We show that genetically identical reciprocal F1 hybrid triploids can display transgenerational epigenetic effects on viable F2 seed development. The success or failure of reproductive outcomes from intra-species crosses between plants of different ploidy levels is an important factor in flowering plant evolution and crop breeding. However, the effects of inter-ploidy cross directions on F1 hybrid offspring fitness are poorly understood. In Arabidopsis thaliana, hybridization between diploid and tetraploid plants can produce viable F1 triploid plants. When selfed, such F1 triploid plants act as aneuploid gamete production "machines" where the vast majority of gametes generated are aneuploid which, following sexual reproduction, can generate aneuploid swarms of F2 progeny (Henry et al. 2009). There is potential for some aneuploids to cause gametophyte abortion and/or F2 seed abortion (Henry et al. 2009). In this study, we analyse the reproductive success of 178 self-fertilized inter-accession F1 hybrid triploids and demonstrate that the proportions of aborted or normally developed F2 seeds from the selfed F1 triploids depend upon a combination of natural variation and cross direction, with strong interaction between these factors. Single-seed ploidy analysis indicates that the embryonic DNA content of phenotypically normal F2 seeds is highly variable and that these DNA content distributions are also affected by genotype and cross direction. Notably, genetically identical reciprocal F1 hybrid triploids display grandparent-of-origin effects on F2 seed set, and hence on the ability to tolerate aneuploidy in F2 seed. There are differences between reciprocal F1 hybrid triploids regarding the proportions of normal and aborted F2 seeds generated, and also for the DNA content averages and distributions of the F2 seeds. To identify genetic variation for tolerance of aneuploidy in F2 seeds, we carried out a GWAS which identified two SNPs, termed MOT and POT, which represent candidate loci for genetic control of the proportion of normal F2 seeds obtained from selfed F1 triploids. Parental and grandparental effects on F2 seeds obtained from selfed F1 triploids can have transgenerational consequences for asymmetric gene flow, emergence of novel genotypes in polyploid populations, and for control of F2 seed set in triploid crops.

Indexed as

PloidiesArabidopsisBiological EvolutionDiploidyEpigenomicsGenome, PlantGenotypeGerm Cells, PlantHybridization, GeneticMagnoliopsidaPhenotypePollinationReproductionSelf-FertilizationTriploidyEpigeneticF1 hybridPlant evolutionReproductionTransgenerational effectTriploid bridge

Identifiers

PMID30903284
PMCPMC6675909
OpenAlexW2923758627

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.