Evidence map›Paper›PMID 30707279›Full record

ArticlePlant reproduction2019

Transcriptomics of manually isolated Amborella trichopoda egg apparatus cells.

María Flores-Tornero, Sebastian Proost, Marek Mutwil, Charles P Scutt, Thomas Dresselhaus, Stefanie Sprunck

Erratum issuedOpen access · hybridAbstract read
PubMed Publisher
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. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. iScience · 2025
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  5. Model Species to Investigate the Origin of Flowers.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  6. DNA methylation dynamics during germline development.Journal of integrative plant biology · 2022
    Review
  7. Article
  8. Article
  9. Flowering plants return to the sea….Journal of experimental botany · 2019
    Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

María Flores-TorneroCell Biology and Plant Biochemistry, Biochemie-Zentrum Regensburg, University of Regensburg, Universitätsstrasse 31, 93053, Regensburg, Germany.
Sebastian ProostMax-Planck Institute for Molecular Plant Physiology, Am Muehlenberg 1, 14476, Potsdam, Germany.
Marek MutwilMax-Planck Institute for Molecular Plant Physiology, Am Muehlenberg 1, 14476, Potsdam, Germany.
Charles P ScuttLaboratoire Reproduction et Développement des Plantes, École Normale Supérieure de Lyon, Université Claude Bernard Lyon 1, CNRS, INRA, Université de Lyon, Lyon, France.
Thomas DresselhausCell Biology and Plant Biochemistry, Biochemie-Zentrum Regensburg, University of Regensburg, Universitätsstrasse 31, 93053, Regensburg, Germany.
Stefanie SprunckCell Biology and Plant Biochemistry, Biochemie-Zentrum Regensburg, University of Regensburg, Universitätsstrasse 31, 93053, Regensburg, Germany. stefanie.sprunck@ur.de.
University of Regensburg · DEMax Planck Institute of Molecular Plant Physiology · DENanyang Technological University · SGUniversité Claude Bernard Lyon 1 · FR

Funding

Deutsche Forschungsgemeinschaft DR 334/12-1
6 · The paper itself

Abstract

key messageA protocol for the isolation of egg apparatus cells from the basal angiosperm Amborella trichopoda to generate RNA-seq data for evolutionary studies of fertilization-associated genes. Sexual reproduction is particularly complex in flowering plants (angiosperms). Studies in eudicot and monocot model species have significantly contributed to our knowledge on cell fate specification of gametophytic cells and on the numerous cellular communication events necessary to deliver the two sperm cells into the embryo sac and to accomplish double fertilization. However, for a deeper understanding of the evolution of these processes, morphological, genomic and gene expression studies in extant basal angiosperms are inevitable. The basal angiosperm Amborella trichopoda is of special importance for evolutionary studies, as it is likely sister to all other living angiosperms. Here, we report about a method to isolate Amborella egg apparatus cells and on genome-wide gene expression profiles in these cells. Our transcriptomics data revealed Amborella-specific genes and genes conserved in eudicots and monocots. Gene products include secreted proteins, such as small cysteine-rich proteins previously reported to act as extracellular signaling molecules with important roles during double fertilization. The detection of transcripts encoding EGG CELL 1 (EC1) and related prolamin-like family proteins in Amborella egg cells demonstrates the potential of the generated data set to study conserved molecular mechanisms and the evolution of fertilization-related genes and their encoded proteins.

Indexed as

Genome, PlantCell SeparationMagnoliopsidaOvuleRNA, PlantTranscriptomeRNA, PlantAmborellaEC1Egg cellMicrodissectionRALFRNA-seqSynergid cell

Identifiers

PMID30707279
OpenAlexW2913273628

What OpenQuestion holds

Textmetadata
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.