Evidence map›Paper›PMID 28944094›Full record

ArticleCellular logistics2017

The ARL2 GTPase regulates mitochondrial fusion from the intermembrane space.

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

Open access · diamondAbstract read
In one paragraph

Article in Cellular logistics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Mechanism-Based Redesign of GAP to Activate Oncogenic Ras.Journal of the American Chemical Society · 2023
    Article
  8. The Arf family GTPases: Regulation of vesicle biogenesis and beyond.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    Review
  9. Article
  10. Article
  11. Roles for ELMOD2 and Rootletin in ciliogenesis.Molecular biology of the cell · 2021
    Article
  12. Review
  13. Article
  14. ARF family GTPases with links to cilia.American journal of physiology. Cell physiology · 2020
    Review
  15. Review
  16. Article
  17. Compositional complexity of rods and rings.Molecular biology of the cell · 2018
    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.

Laura E NewmanDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA, USA.
Cara R SchiavonDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA, USA.
Rachel E TurnDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA, USA.
Richard A KahnDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA, USA.
Emory University · US

Funding

Training Program in Biochemistry, Cell and Molecular BiologyT32GM008367 · NIGMS · EMORY UNIVERSITY · PI BOISE, LAWRENCE H., CORBETT, ANITA H. · 1990 to 2019
$5.6M
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
NCI NIH HHS F31 CA236493NIGMS NIH HHS R01 GM090158NIGMS NIH HHS R35 GM122568NIGMS NIH HHS T32 GM008367
6 · The paper itself

Abstract

Mitochondria are essential, dynamic organelles that regularly undergo both fusion and fission in response to cellular conditions, though mechanisms of the regulation of their dynamics are incompletely understood. We provide evidence that increased activity of the small GTPase ARL2 is strongly correlated with an increase in fusion, while loss of ARL2 activity results in a decreased rate of mitochondrial fusion. Strikingly, expression of activated ARL2 can partially restore the loss of fusion resulting from deletion of either mitofusin 1 (MFN1) or mitofusin 2 (MFN2), but not deletion of both. We only observe the full effects of ARL2 on mitochondrial fusion when it is present in the intermembrane space (IMS), as constructs driven to the matrix or prevented from entering mitochondria are essentially inactive in promoting fusion. Thus, ARL2 is the first regulatory (small) GTPase shown to act inside mitochondria or in the fusion pathway. Finally, using high-resolution, structured illumination microscopy (SIM), we find that ARL2 and mitofusin immunoreactivities present as punctate staining along mitochondria that share a spatial convergence in fluorescence signals. Thus, we propose that ARL2 plays a regulatory role in mitochondrial fusion, acting from the IMS and requiring at least one of the mitofusins in their canonical role in fusion of the outer membranes.

Indexed as

ADP-ribosylation factor (ARF) like 2ARL2cell cultureGTPaseGTPase activating protein (GAP)intermembrane spacemembrane fusionMFN1MFN2mitochondriamitofusin 1mitofusin 2SIMstructured illumination microscopy

Identifiers

PMID28944094
PMCPMC5602422
OpenAlexW2644963672

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.