Evidence map›Paper›PMID 40000850›Full record

ArticleNature cell biology2025

ER-to-Golgi trafficking through a dynamic intermediate cis-Golgi tubular network in Arabidopsis.

Louise Fougère, Magali Grison, Patricia Laquel, Matheus Montrazi, Fabrice Cordelières, Mónica Fernández-Monreal, Christel Poujol, Tomohiro Uemura, Akihiko Nakano, Yoko Ito and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Mechanobiological Dynamics-Inspired Mechanomodulatory Biomaterials.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  6. Review
  7. Article
  8. Review
  9. Trafficking and localization of Golgi-residentFrontiers in plant science · 2025
    Review
  10. Article
  11. 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

11 authors.

Louise Fougère *Laboratoire de Biogenèse Membranaire, Université de Bordeaux, CNRS UMR5200, Villenave d'Ornon, France.ORCID http://orcid.org/0009-0009-1004-4502
Magali Grison *Laboratoire de Biogenèse Membranaire, Université de Bordeaux, CNRS UMR5200, Villenave d'Ornon, France.ORCID http://orcid.org/0000-0002-3080-3686
Patricia LaquelLaboratoire de Biogenèse Membranaire, Université de Bordeaux, CNRS UMR5200, Villenave d'Ornon, France.
Matheus MontraziLaboratoire de Biogenèse Membranaire, Université de Bordeaux, CNRS UMR5200, Villenave d'Ornon, France.
Fabrice CordelièresBordeaux Imaging Center (BIC), Université de Bordeaux, INSERM, CNRS UAR3420, Bordeaux, France.ORCID http://orcid.org/0000-0002-5383-5816
Mónica Fernández-MonrealBordeaux Imaging Center (BIC), Université de Bordeaux, INSERM, CNRS UAR3420, Bordeaux, France.ORCID http://orcid.org/0000-0001-7278-448X
Christel PoujolBordeaux Imaging Center (BIC), Université de Bordeaux, INSERM, CNRS UAR3420, Bordeaux, France.ORCID http://orcid.org/0000-0002-5222-9064
Tomohiro UemuraFaculty of Core Research, Natural Science Division, Ochanomizu University, Tokyo, Japan.ORCID http://orcid.org/0000-0001-7270-7986
Akihiko NakanoLive Cell Super-Resolution Imaging Research Team, RIKEN Center for Advanced Photonics, Wako, Saitama, Japan.ORCID http://orcid.org/0000-0003-3635-548X
Yoko ItoInstitute for Human Life Science, Ochanomizu University, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9877-1596
Yohann BouttéLaboratoire de Biogenèse Membranaire, Université de Bordeaux, CNRS UMR5200, Villenave d'Ornon, France. yohann.boutte@u-bordeaux.fr.ORCID http://orcid.org/0000-0002-7555-074X

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-INSB-04Agence Nationale de la Recherche (French National Research Agency) ANR-18-CE13-0025Agence Nationale de la Recherche (French National Research Agency) ANR-21-CE13-0019
6 · The paper itself

Abstract

Endoplasmic reticulum (ER)-to-Golgi trafficking is a central process of the secretory system of eukaryotic cells that ensures proper spatiotemporal sorting of proteins and lipids. However, the nature of the ER-Golgi intermediate compartments (ERGICs) and the molecular mechanisms mediating the transition between ERGICs and the Golgi, as well as the universality of these processes among eukaryotes, remain undiscovered. Here we identify a reticulated tubulo-vesicular network, labelled by MEMBRIN proteins, that is mostly independent of the Golgi, highly dynamic at the ER-Golgi interface and crossed by ER-induced released luminal cargos. We find that plant ERGICs become stabilized by the interaction they establish with pre-existing Golgi and gradually mature into Golgi cisternae, this process being dependent on C24-ceramide sphingolipids. Our study is a major twist in the understanding of the Golgi, as it identifies that the ERGICs in plants comprise a Golgi-independent and highly dynamic tubular network from which arise more stable Golgi-associated pre-cisternae structures.

Indexed as

ArabidopsisEndoplasmic ReticulumGolgi ApparatusArabidopsis ProteinsCeramidesProtein TransportSphingolipidsArabidopsis ProteinsCeramidesSphingolipids

Identifiers

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.