Evidence map›Paper›PMID 28559542›Full record

ArticleImmunology and cell biology2017

MARCH9-mediated ubiquitination regulates MHC I export from the TGN.

Francesca De Angelis Rigotti, Aude De Gassart, Carina Pforr, Florencia Cano, Prudence N'Guessan, Alexis Combes, Voahirana Camossetto, Paul J Lehner, Philippe Pierre, Evelina Gatti

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In one paragraph

Article in Immunology and cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. MARCH E3 Ligases: Understudied Regulators of Pulmonary Immune Function.Journal of respiratory biology and translational medicine · 2026
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  6. IL-6-Driven Autocrine Lactate Promotes Immune Escape of Uveal Melanoma.Investigative ophthalmology & visual science · 2024
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  12. The RING finger protein family in health and disease.Signal transduction and targeted therapy · 2022
    Review
  13. Article
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  17. Review
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Francesca De Angelis RigottiCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Aude De GassartCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Carina PforrCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Florencia CanoDivision of Immunology, Cambridge Institute of Medical Research, Addenbrookes Hospital, Cambridge, UK.
Prudence N'GuessanCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Alexis CombesCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Voahirana CamossettoCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Paul J LehnerDivision of Immunology, Cambridge Institute of Medical Research, Addenbrookes Hospital, Cambridge, UK.
Philippe PierreCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Evelina GattiCentre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, CNRS, INSERM, Marseille, France.
Aix-Marseille Université · FRAddenbrooke's Hospital · GBCentre d’Immunologie de Marseille-Luminy · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the heterogeneous nature of antigens, major histocompatibility complex class I (MHC I) intracellular transport intersects with multiple degradation pathways for efficient peptide loading and presentation to cytotoxic T cells. MHC I loading with peptides in the endoplasmic reticulum (ER) is a tightly regulated process, while post-ER intracellular transport is considered to occur by default, leading to peptide-bearing MHC I delivery to the plasma membrane. We show here that MHC I traffic is submitted to a previously uncharacterized sorting step at the trans Golgi network (TGN), dependent on the ubiquitination of its cytoplasmic tail lysine residues. MHC I ubiquitination is mediated by the E3 ligase membrane-associated RING-CH 9 (MARCH9) and allows MHC I access to Syntaxin 6-positive endosomal compartments. We further show that MARCH9 can also target the human MHC I-like lipid antigen-presentation molecule CD1a. MARCH9 expression is modulated by microbial pattern exposure in dendritic cells (DCs), thus revealing the role of this ubiquitin E3 ligase in coordinating MHC I access to endosomes and DC activation for efficient antigen cross-presentation.

Indexed as

Antigen PresentationAntigens, CD1Cell MembraneCells, CulturedDendritic CellsEndoplasmic ReticulumEndosomesHistocompatibility Antigens Class IHLA AntigensHumansMembrane ProteinsMonocytesProtein DomainsProtein Sorting SignalsProtein TransportQa-SNARE ProteinsAntigens, CD1CD1a antigenHistocompatibility Antigens Class IHLA AntigensMARCHF9 protein, humanMembrane ProteinsProtein Sorting SignalsQa-SNARE ProteinsSTX6 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID28559542
OpenAlexW2616943568

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.