Evidence map›Paper›PMID 28254827›Full record

ArticleThe Journal of cell biology2017

The MICOS component Mic60 displays a conserved membrane-bending activity that is necessary for normal cristae morphology.

Daryna Tarasenko, Mariam Barbot, Daniel C Jans, Benjamin Kroppen, Boguslawa Sadowski, Gudrun Heim, Wiebke Möbius, Stefan Jakobs, Michael Meinecke

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 117 citations in OpenAlex.

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  12. Molecular machineries shaping the mitochondrial inner membrane.Nature reviews. Molecular cell biology · 2025
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3 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 1 country.

Daryna TarasenkoDepartment of Cellular Biochemistry, University Medical Center Göttingen, 37073 Göttingen, Germany.
Mariam BarbotDepartment of Cellular Biochemistry, University Medical Center Göttingen, 37073 Göttingen, Germany.ORCID 0000-0003-3293-6623
Daniel C JansDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-6356-9742
Benjamin KroppenDepartment of Cellular Biochemistry, University Medical Center Göttingen, 37073 Göttingen, Germany.
Boguslawa SadowskiDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, 37075 Göttingen, Germany.ORCID 0000-0001-9888-4059
Gudrun HeimElectron Microscopy Facility, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Wiebke MöbiusDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, 37075 Göttingen, Germany.ORCID 0000-0002-2902-7165
Stefan JakobsDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-8028-3121
Michael MeineckeDepartment of Cellular Biochemistry, University Medical Center Göttingen, 37073 Göttingen, Germany michael.meinecke@med.uni-goettingen.de.ORCID 0000-0003-1414-6951
Universitätsmedizin Göttingen · DENanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 · DEMax Planck Institute for Biophysical Chemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inner membrane (IM) of mitochondria displays an intricate, highly folded architecture and can be divided into two domains: the inner boundary membrane adjacent to the outer membrane and invaginations toward the matrix, called cristae. Both domains are connected by narrow, tubular membrane segments called cristae junctions (CJs). The formation and maintenance of CJs is of vital importance for the organization of the mitochondrial IM and for mitochondrial and cellular physiology. The multisubunit mitochondrial contact site and cristae organizing system (MICOS) was found to be a major factor in CJ formation. In this study, we show that the MICOS core component Mic60 actively bends membranes and, when inserted into prokaryotic membranes, induces the formation of cristae-like plasma membrane invaginations. The intermembrane space domain of Mic60 has a lipid-binding capacity and induces membrane curvature even in the absence of the transmembrane helix. Mic60 homologues from α-proteobacteria display the same membrane deforming activity and are able to partially overcome the deletion of Mic60 in eukaryotic cells. Our results show that membrane bending by Mic60 is an ancient mechanism, important for cristae formation, and had already evolved before α-proteobacteria developed into mitochondria.

Indexed as

Biological TransportEukaryotic CellsMitochondriaMitochondrial MembranesMitochondrial Membrane Transport ProteinsMitochondrial ProteinsProtein BindingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsMitochondrial Membrane Transport ProteinsMitochondrial ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID28254827
PMCPMC5379949
OpenAlexW2594660835

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.