Evidence map›Paper›PMID 37815982›Full record

ArticlePloS one2023

Evolution and development of fruits of Erycina pusilla and other orchid species.

Dewi Pramanik, Annette Becker, Clemens Roessner, Oliver Rupp, Diego Bogarín, Oscar Alejandro Pérez-Escobar, Anita Dirks-Mulder, Kevin Droppert, Alexander Kocyan, Erik Smets and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

11 authors at 6 institutions in 7 countries.

Dewi PramanikEvolutionary Ecology Group, Naturalis Biodiversity Center, Leiden, The Netherlands.ORCID 0000-0002-6781-774X
Annette BeckerDevelopment Biology of Plants, Institute for Botany, Justus-Liebig-University Giessen, Giessen, Germany.
Clemens RoessnerDevelopment Biology of Plants, Institute for Botany, Justus-Liebig-University Giessen, Giessen, Germany.
Oliver RuppDepartment of Bioinformatics and Systems Biology, Justus Liebig University, Giessen, Germany.ORCID 0000-0003-2755-6458
Diego BogarínEvolutionary Ecology Group, Naturalis Biodiversity Center, Leiden, The Netherlands.
Oscar Alejandro Pérez-EscobarComparative Plant and Fungal Biology, Royal Botanicals Gardens, Kew Richmond Surrey, London, United Kingdom.
Anita Dirks-MulderFaculty of Science and Technology, University of Applied Sciences Leiden, Leiden, The Netherlands.
Kevin DroppertFaculty of Science and Technology, University of Applied Sciences Leiden, Leiden, The Netherlands.
Alexander KocyanBotanical Museum, Department of Plant and Microbial Biology, University of Zurich, Zurich, Switzerland.
Erik SmetsEvolutionary Ecology Group, Naturalis Biodiversity Center, Leiden, The Netherlands.ORCID 0000-0002-9416-983X
Barbara GravendeelEvolutionary Ecology Group, Naturalis Biodiversity Center, Leiden, The Netherlands.
Justus-Liebig-Universität Gießen · DELeiden University · NLUniversity of Applied Sciences Leiden · NLNaturalis Biodiversity Center · NLRoyal Botanic Gardens, Kew · GBUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fruits play a crucial role in seed dispersal. They open along dehiscence zones. Fruit dehiscence zone formation has been intensively studied in Arabidopsis thaliana. However, little is known about the mechanisms and genes involved in the formation of fruit dehiscence zones in species outside the Brassicaceae. The dehiscence zone of A. thaliana contains a lignified layer, while dehiscence zone tissues of the emerging orchid model Erycina pusilla include a lipid layer. Here we present an analysis of evolution and development of fruit dehiscence zones in orchids. We performed ancestral state reconstructions across the five orchid subfamilies to study the evolution of selected fruit traits and explored dehiscence zone developmental genes using RNA-seq and qPCR. We found that erect dehiscent fruits with non-lignified dehiscence zones and a short ripening period are ancestral characters in orchids. Lignified dehiscence zones in orchid fruits evolved multiple times from non-lignified zones. Furthermore, we carried out gene expression analysis of tissues from different developmental stages of E. pusilla fruits. We found that fruit dehiscence genes from the MADS-box gene family and other important regulators in E. pusilla differed in their expression pattern from their homologs in A. thaliana. This suggests that the current A. thaliana fruit dehiscence model requires adjustment for orchids. Additionally, we discovered that homologs of A. thaliana genes involved in the development of carpel, gynoecium and ovules, and genes involved in lipid biosynthesis were expressed in the fruit valves of E. pusilla, implying that these genes may play a novel role in formation of dehiscence zone tissues in orchids. Future functional analysis of developmental regulators, lipid identification and quantification can shed more light on lipid-layer based dehiscence of orchid fruits.

Indexed as

ArabidopsisBrassicaceaeFruitGene Expression ProfilingGene Expression Regulation, PlantLipidsLipids

Identifiers

PMID37815982
PMCPMC10564159
OpenAlexW4387504474

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.