Evidence map›Paper›PMID 42095818›Full record

ArticleThe Journal of cell biology2026

Mitochondrially tethered Mmm1 can function as a sole lipid transporter at ER-mitochondria contacts.

Christian Covill-Cooke, Takashi Hirashima, Shin Kawano, Joe Ganellin, Andrew Moody, Sabine N S van Schie, Arun T John Peter, Chika Horie Saito, Toshiya Endo, Benoît Kornmann

Abstract read
In one paragraph

Article in The Journal of cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Christian Covill-Cooke *Department of Biochemistry, University of Oxford, Oxford, UK.ORCID 0000-0002-4479-8734
Takashi Hirashima *Faculty of Life Sciences, Kyoto Sangyo University , Kyoto, Japan.ORCID 0000-0002-9144-6045
Shin Kawano *Faculty of Life Sciences, Kyoto Sangyo University , Kyoto, Japan.ORCID 0009-0003-2856-5468
Joe GanellinDepartment of Biochemistry, University of Oxford, Oxford, UK.ORCID 0009-0003-8633-7674
Andrew MoodyDepartment of Biochemistry, University of Oxford, Oxford, UK.ORCID 0009-0008-7211-2876
Sabine N S van SchieInstitute of Biochemistry, ETH Zurich , Zurich, Switzerland.ORCID 0000-0002-5294-7779
Arun T John PeterInstitute of Biochemistry, ETH Zurich , Zurich, Switzerland.ORCID 0000-0001-8356-5469
Chika Horie SaitoFaculty of Life Sciences, Kyoto Sangyo University , Kyoto, Japan.ORCID 0009-0002-5054-8106
Toshiya EndoFaculty of Life Sciences, Kyoto Sangyo University , Kyoto, Japan.ORCID 0000-0001-8548-1584
Benoît KornmannDepartment of Biochemistry, University of Oxford, Oxford, UK.ORCID 0000-0002-6030-8555

Funding

EPA Cephalosporin Fund CF 412Japan Agency for Medical Research and Development 21gm1410002h0002Japan Science and Technology Agency JPMJCR12M1Japan Society for the Promotion of Science 15H05705Japan Society for the Promotion of Science 17K18230Japan Society for the Promotion of Science 20H04912Japan Society for the Promotion of Science 20H05689Japan Society for the Promotion of Science 20H05929Japan Society for the Promotion of Science 2222703Japan Society for the Promotion of Science 25840020Japan Society for the Promotion of Science 25H00978Japan Society for the Promotion of Science 25H21752Japan Society of the Promotion of Science 23KJ2067Takeda Science FoundationWellcome Trust 091911/B/10/ZWellcome Trust 107457/Z/15/ZWellcome Trust 214291/Z/18/Z
6 · The paper itself

Abstract

Yeast mitochondria receive the majority of their lipids from the ER via the heterotetrameric ERMES lipid transport complex. This complex is thought to establish a lipid-transporting bridge of fixed composition spanning the space between both organelles. Intriguingly, however, some of the lipid-transporting components of the complex can be replaced by an artificial ER-mitochondria tether without lipid transport activity, questioning ERMES' relevance in lipid transport. Here, we show that Mmm1, one of the four ERMES subunits, alone is sufficient to support ERMES function when it is artificially tethered to mitochondria, provided its lipid-binding domain is intact. Combined with our previous finding that the absence of Mdm12 and Mdm34 can be rescued by the presence of Mmm1 and the artificial tethering protein ChiMERA, our results suggest that Mmm1 can act as the sole lipid transporter at the ER-mitochondrial contact sites, provided that Mdm10 is present, even in the absence of the other two subunits. Thus, our work reconciles ERMES' importance in lipid transport with the fact that the lipid transport activity of some of its components is not strictly necessary for function.

Indexed as

Endoplasmic ReticulumLipid MetabolismMembrane ProteinsMitochondriaMitochondrial ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsBiological TransportMitochondria Associated MembranesMDM10 protein, S cerevisiaeMdm12 protein, S cerevisiaeMembrane ProteinsMitochondrial ProteinsMMM1 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID42095818
PMCPMC13151913

What OpenQuestion holds

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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.