Evidence map›Paper›PMID 30865555›Full record

ArticleMolecular biology of the cell2019

ELMOD2 regulates mitochondrial fusion in a mitofusin-dependent manner, downstream of ARL2.

Cara R Schiavon, Rachel E Turn, Laura E Newman, Richard A Kahn

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Arf family GTPases: Regulation of vesicle biogenesis and beyond.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Roles for ELMOD2 and Rootletin in ciliogenesis.Molecular biology of the cell · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. 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 2 institutions in 1 country.

Cara R SchiavonCancer Biology and bBiochemistry, Cell, and Developmental Biology Graduate Programs, Graduate Division of Biomedical and Biological Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322.
Rachel E TurnCancer Biology and bBiochemistry, Cell, and Developmental Biology Graduate Programs, Graduate Division of Biomedical and Biological Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322.
Laura E NewmanSalk Institute for Biological Studies, La Jolla, CA 92037.
Richard A KahnDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322.
Emory University · USSalk Institute for Biological Studies · US

Funding

ENNCF - Viral Vector CoreP30NS055077 · NINDS · EMORY UNIVERSITY · PI BASSELL, GARY J · 2008 to 2018
$6.8M
Molecular mechanisms of ARF family GTPasesR35GM122568 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2017 to 2024
$3.7M
The Regulation and Cellular Activities of the ARL2 GTPaseR01GM090158 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2010 to 2017
$2.5M
ELMOD2: proposed roles in regulating mitochondrial fusion and cell cycleF31CA236493 · NCI · EMORY UNIVERSITY · PI TURN, RACHEL ELIZABETH · 2019 to 2021
$137k
Regulation of mitochondrial function by ARL2 and its putative effector ELMOD2F31GM111047 · NIGMS · EMORY UNIVERSITY · PI NEWMAN, LAURA ELIZABETH · 2014 to 2017
$92k
NCI NIH HHS F31 CA236493NIGMS NIH HHS F31 GM111047NIGMS NIH HHS R01 GM090158NIGMS NIH HHS R35 GM122568NINDS NIH HHS P30 NS055077
6 · The paper itself

Abstract

Mitochondria are essential and dynamic organelles undergoing constant fission and fusion. The primary players in mitochondrial morphology (MFN1/2, OPA1, DRP1) have been identified, but their mechanism(s) of regulation are still being elucidated. ARL2 is a regulatory GTPase that has previously been shown to play a role in the regulation of mitochondrial morphology. Here we demonstrate that ELMOD2, an ARL2 GTPase-activating protein (GAP), is necessary for ARL2 to promote mitochondrial elongation. We show that loss of ELMOD2 causes mitochondrial fragmentation and a lower rate of mitochondrial fusion, while ELMOD2 overexpression promotes mitochondrial tubulation and increases the rate of fusion in a mitofusin-dependent manner. We also show that a mutant of ELMOD2 lacking GAP activity is capable of promoting fusion, suggesting that ELMOD2 does not need GAP activity to influence mitochondrial morphology. Finally, we show that ELMOD2, ARL2, Mitofusins 1 and 2, Miros 1 and 2, and mitochondrial phospholipase D (mitoPLD) all localize to discrete, regularly spaced puncta along mitochondria. These results suggest that ELMOD2 is functioning as an effector downstream of ARL2 and upstream of the mitofusins to promote mitochondrial fusion. Our data provide insights into the pathway by which mitochondrial fusion is regulated in the cell.

Indexed as

AnimalsCell LineChlorocebus aethiopsCOS CellsCytoskeletal ProteinsGene Knockout TechniquesGTP-Binding ProteinsGTP PhosphohydrolasesHumansMembrane FusionMiceMicrotubule-Associated ProteinsMitochondriaMitochondrial DynamicsMitochondrial MembranesMitochondrial ProteinsARL2 protein, humanCytoskeletal ProteinsELMOD2 protein, humanGTP-Binding ProteinsGTP PhosphohydrolasesMicrotubule-Associated ProteinsMitochondrial ProteinsmitoPLD protein, humanPhospholipase D

Identifiers

PMID30865555
PMCPMC6724520
OpenAlexW2921793557

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.