Evidence map›Paper›PMID 24951481›Full record

ArticleThe Plant cell2014

Plasticity in Cell Division Patterns and Auxin Transport Dependency during in Vitro Embryogenesis in Brassica napus.

Mercedes Soriano, Hui Li, Cédric Jacquard, Gerco C Angenent, Joan Krochko, Remko Offringa, Kim Boutilier

Open access · greenAbstract read
In one paragraph

Article in The Plant cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.1field-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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Establishment and maintenance of embryogenic cell fate during microspore embryogenesis.The Plant journal : for cell and molecular biology · 2025
    Article
  5. The maternal embrace: the protection of plant embryos.Journal of experimental botany · 2024
    Review
  6. Article
  7. Current issues in molecular biology · 2023
    Review
  8. Article
  9. Article
  10. BABY BOOM regulates early embryo and endosperm development.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Embryogenesis of European Radish (Plants (Basel, Switzerland) · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Identification, Gene Structure, and Expression ofFrontiers in plant science · 2020
    Article
  19. Review
  20. 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

7 authors at 4 institutions in 3 countries.

Mercedes SorianoPlant Research International, 6700 AP Wageningen, The Netherlands.
Hui LiPlant Research International, 6700 AP Wageningen, The Netherlands.
Cédric JacquardUniversité de Reims Champagne-Ardenne, Unité de Recherche Vignes et Vins de Champagne-EA 4707, Laboratoire de Stress, Défenses et Reproduction des Plantes, Moulin de la Housse, 51687 REIMS Cedex 2, France.
Gerco C AngenentPlant Research International, 6700 AP Wageningen, The Netherlands Laboratory for Molecular Biology, Wageningen University, 6708 PB, Wageningen, The Netherlands.
Joan KrochkoPlant Biotechnology Institute, National Research Council of Canada, Saskatoon S7N 0W9, Canada.
Remko OffringaMolecular and Developmental Genetics, Institute Biology Leiden, Leiden University, 2333 BE Leiden, The Netherlands.
Kim BoutilierPlant Research International, 6700 AP Wageningen, The Netherlands kim.boutilier@wur.nl.
Leiden University · NLPlant Biotechnology Institute · CAUniversité de Reims Champagne-Ardenne · FRWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In Arabidopsis thaliana, zygotic embryo divisions are highly regular, but it is not clear how embryo patterning is established in species or culture systems with irregular cell divisions. We investigated this using the Brassica napus microspore embryogenesis system, where the male gametophyte is reprogrammed in vitro to form haploid embryos in the absence of exogenous growth regulators. Microspore embryos are formed via two pathways: a zygotic-like pathway, characterized by initial suspensor formation followed by embryo proper formation from the distal cell of the suspensor, and a pathway characterized by initially unorganized embryos lacking a suspensor. Using embryo fate and auxin markers, we show that the zygotic-like pathway requires polar auxin transport for embryo proper specification from the suspensor, while the suspensorless pathway is polar auxin transport independent and marked by an initial auxin maximum, suggesting early embryo proper establishment in the absence of a basal suspensor. Polarity establishment in this suspensorless pathway was triggered and guided by rupture of the pollen exine. Irregular division patterns did not affect cell fate establishment in either pathway. These results confirm the importance of the suspensor and suspensor-driven auxin transport in patterning, but also uncover a mechanism where cell patterning is less regular and independent of auxin transport.

Identifiers

PMID24951481
PMCPMC4114952
OpenAlexW2153031454

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.