Evidence map›Paper›PMID 28628083›Full record

ArticleNature cell biology2017

Molecular basis of selective mitochondrial fusion by heterotypic action between OPA1 and cardiolipin.

Tadato Ban, Takaya Ishihara, Hiroto Kohno, Shotaro Saita, Ayaka Ichimura, Katsumi Maenaka, Toshihiko Oka, Katsuyoshi Mihara, Naotada Ishihara

Abstract read
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In one paragraph

Article in Nature cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 238 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
238citing papers in PubMed, 3 pooled it
15.2field-weighted citation impact, top 1% 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

238 citing papers in PubMed, 3 syntheses or guidelines pooled it, 402 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Stay in touch with the endoplasmic reticulum.Science China. Life sciences · 2024
    Pooled it
  4. Review
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  16. Disruption of Hepatic Insulin Signaling Causes Phospholipid Dysregulation in Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  17. Decoding the Role of Lipid Metabolism and Membrane Dynamics in Melanoma.International journal of molecular sciences · 2026
    Review
  18. Article
  19. Chemo-/radiotherapy-induced cardiomyopathy: roles of mitochondria and endoplasmic reticulum.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
    Review
  20. Article

178 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Tadato BanDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.
Takaya IshiharaDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.
Hiroto KohnoDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.
Shotaro SaitaDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.
Ayaka IchimuraDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.
Katsumi MaenakaLaboratory of Biomolecular Science, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.ORCID http://orcid.org/0000-0002-5459-521X
Toshihiko OkaDepartment of Life Science, Rikkyo University, Tokyo 171-8501, Japan.
Katsuyoshi MiharaDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.
Naotada IshiharaDepartment of Protein Biochemistry, Institute of Life Science, Kurume University, Kurume 839-0864, Japan.ORCID http://orcid.org/0000-0002-6305-7149
Kurume University · JPHokkaido University · JPRikkyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria are highly dynamic organelles that undergo frequent fusion and fission. Optic atrophy 1 (OPA1) is an essential GTPase protein for both mitochondrial inner membrane (IM) fusion and cristae morphology. Under mitochondria-stress conditions, membrane-anchored L-OPA1 is proteolytically cleaved to form peripheral S-OPA1, leading to the selection of damaged mitochondria for mitophagy. However, molecular details of the selective mitochondrial fusion are less well understood. Here, we showed that L-OPA1 and cardiolipin (CL) cooperate in heterotypic mitochondrial IM fusion. We reconstituted an in vitro membrane fusion reaction using purified human L-OPA1 protein expressed in silkworm, and found that L-OPA1 on one side of the membrane and CL on the other side are sufficient for fusion. GTP-independent membrane tethering through L-OPA1 and CL primes the subsequent GTP-hydrolysis-dependent fusion, which can be modulated by the presence of S-OPA1. These results unveil the most minimal intracellular membrane fusion machinery. In contrast, independent of CL, a homotypic trans-OPA1 interaction mediates membrane tethering, thereby supporting the cristae structure. Thus, multiple OPA1 functions are modulated by local CL conditions for regulation of mitochondrial morphology and quality control.

Indexed as

Mitochondrial DynamicsAnimalsAnimals, Genetically ModifiedBombyxCardiolipinsGene TargetingGTP PhosphohydrolasesGuanosine TriphosphateHeLa CellsHumansHydrolysisLiposomesMitochondriaMitochondrial MembranesProtein BindingProtein Interaction Domains and MotifsCardiolipinsGTP PhosphohydrolasesGuanosine TriphosphateLiposomesOPA1 protein, humanRecombinant Proteins

Identifiers

PMID28628083
OpenAlexW2626238074

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.