Evidence map›Paper›PMID 23615445›Full record

ArticleMolecular biology of the cell2013

Effects of Fcj1-Mos1 and mitochondrial division on aggregation of mitochondrial DNA nucleoids and organelle morphology.

Kie Itoh, Yasushi Tamura, Miho Iijima, Hiromi Sesaki

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Molecular machineries shaping the mitochondrial inner membrane.Nature reviews. Molecular cell biology · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. An AAA-ATPase links mitochondrial division with DNA nucleoids.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. Biology open · 2020
    Article
  14. Review
  15. Review
  16. Mitochondrial proteins: from biogenesis to functional networks.Nature reviews. Molecular cell biology · 2019
    Review
  17. Review
  18. Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Kie ItohDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Yasushi Tamura
Miho Iijima
Hiromi Sesaki
Johns Hopkins University · US

Funding

Lipid Signaling in ChemotaxisR01GM084015 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI IIJIMA, MIHO · 2009 to 2019
$2.9M
Mitochondrial Fusion and DivisionR01GM089853 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SESAKI, HIROMI · 2010 to 2014
$2.1M
Introducing Mitochondrial Stasis in NeuronsR21NS084154 · NINDS · JOHNS HOPKINS UNIVERSITY · PI SESAKI, HIROMI · 2013 to 2014
$443k
NIGMS NIH HHS GM084015NIGMS NIH HHS GM089853NIGMS NIH HHS R01 GM084015NIGMS NIH HHS R01 GM089853NINDS NIH HHS R21 NS084154
6 · The paper itself

Abstract

Mitochondrial DNA (mtDNA) is packaged into DNA-protein complexes called nucleoids, which are distributed as many small foci in mitochondria. Nucleoids are crucial for the biogenesis and function of mtDNA. Here, using a yeast genetic screen for components that control nucleoid distribution and size, we identify Fcj1 and Mos1, two evolutionarily conserved mitochondrial proteins that maintain the connection between the cristae and boundary membranes. These two proteins are also important for establishing tubular morphology of mitochondria, as mitochondria lacking Fcj1 and Mos1 form lamellar sheets. We find that nucleoids aggregate, increase in size, and decrease in number in fcj1 and mos1 cells. In addition, Fcj1 form punctate structures and localized adjacent to nucleoids. Moreover, connecting mitochondria by deleting the DNM1 gene required for organelle division enhances aggregation of mtDNA nucleoids in fcj1 and mos1 cells, whereas single deletion of DNM1 does not affect nucleoids. Conversely, deleting F1Fo-ATP synthase dimerization factors generates concentric ring-like cristae, restores tubular mitochondrial morphology, and suppresses nucleoid aggregation in these mutants. Our findings suggest an unexpected role of Fcj1-Mos1 and organelle division in maintaining the distribution and size of mtDNA nucleoids.

Indexed as

DNA, MitochondrialGenome, MitochondrialImmunoblottingLuminescent ProteinsMembrane ProteinsMicroscopy, Electron, TransmissionMicroscopy, FluorescenceMitochondriaMitochondrial DynamicsMitochondrial ProteinsMitochondrial Proton-Translocating ATPasesMutationProton-Translocating ATPasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsATP20 protein, S cerevisiaeDNA, MitochondrialFcj1 protein, S cerevisiaeLuminescent ProteinsMembrane ProteinsMIC10 protein, S cerevisiaeMitochondrial ProteinsMitochondrial Proton-Translocating ATPasesProton-Translocating ATPasesSaccharomyces cerevisiae ProteinsTIM11 protein, S cerevisiae

Identifiers

PMID23615445
PMCPMC3681690
OpenAlexW2109371989

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.