Evidence map›Paper›PMID 29982367›Full record

ArticleAnnals of botany2018

Establishing the cell biology of apomictic reproduction in diploid Boechera stricta (Brassicaceae).

Joanna Rojek, Malgorzata Kapusta, Malgorzata Kozieradzka-Kiszkurno, Daria Majcher, Marcin Górniak, Elwira Sliwinska, Timothy F Sharbel, Jerzy Bohdanowicz

Open access · hybridAbstract read
In one paragraph

Article in Annals of botany, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.2field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  17. Apospory and Diplospory in DiploidFrontiers in plant science · 2019
    Article
  18. TheFrontiers in plant science · 2019
    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

8 authors at 3 institutions in 2 countries.

Joanna RojekDepartment of Plant Cytology and Embryology, Faculty of Biology, University of Gdansk, Poland.
Malgorzata KapustaDepartment of Plant Cytology and Embryology, Faculty of Biology, University of Gdansk, Poland.
Malgorzata Kozieradzka-KiszkurnoDepartment of Plant Cytology and Embryology, Faculty of Biology, University of Gdansk, Poland.
Daria MajcherDepartment of Plant Cytology and Embryology, Faculty of Biology, University of Gdansk, Poland.
Marcin GórniakDepartment of Molecular Evolution, Faculty of Biology, University of Gdansk, Poland.
Elwira SliwinskaLaboratory of Molecular Biology and Cytometry, Department of Agricultural Biotechnology, UTP University of Technology and Life Sciences in Bydgoszcz, Poland.
Timothy F SharbelGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Jerzy BohdanowiczDepartment of Plant Cytology and Embryology, Faculty of Biology, University of Gdansk, Poland.
University of Gdańsk · PLBydgoszcz University of Science and Technology · PLUniversity of Saskatchewan · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: In the Brassicaceae family, apomictic development is characteristic of the genus Boechera. Hybridization, polyploidy and environmental adaptation that arose during the evolution of Boechera may serve as (epi)genetic regulators of apomictic initiation in this genus. Here we focus on Boechera stricta, a predominantly diploid species that reproduces sexually. However, apomictic development in this species has been reported in several studies, indicating non-obligate sexuality. Methods: A progressive investigation of flower development was conducted using three accessions to assess the reproductive system of B. stricta. We employed molecular and cyto-embryological identification using histochemistry, transmission electron microscopy and Nomarski and epifluorescence microscopy. Key Results: Data from internal transcribed spacer (ITS) and chloroplast haplotype sequencing, in addition to microsatellite variation, confirmed the B. stricta genotype for all lines. Embryological data indicated irregularities in sexual reproduction manifested by heterochronic ovule development, longevity of meiocyte and dyad stages, diverse callose accumulation during meiocyte-to-gametophyte development, and the formation of triads and tetrads in several patterns. The arabinogalactan-related sugar epitope recognized by JIM13 immunolocalized to one or more megaspores. Furthermore, pollen sterility and a high frequency of seed abortion appeared to accompany reproduction of the accession ES512, along with the initiation of parthenogenesis. Data from flow cytometric screening revealed both sexual and apomictic seed formation. Conclusion: These results imply that B. stricta is a species with an underlying ability to initiate apomixis, at least with respect to the lines examined here. The existence of apomixis in an otherwise diploid sexual B. stricta may provide the genomic building blocks for establishing highly penetrant apomictic diploids and hybrid relatives. Our findings demonstrate that apomixis per se is a variable trait upon which natural selection could act.

Indexed as

DiploidyApomixisBrassicaceaeGenome, PlantGenotypeHybridization, GeneticMicrosatellite RepeatsOvulePhenotypePollenPolyploidySeedsSelection, Genetic

Identifiers

PMID29982367
PMCPMC6153484
OpenAlexW2894053576

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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.