Evidence map›Paper›PMID 30059502›Full record

ArticlePLoS genetics2018

Ras-ERK-ETS inhibition alleviates neuronal mitochondrial dysfunction by reprogramming mitochondrial retrograde signaling.

Olivia F Duncan, Lucy Granat, Ramya Ranganathan, Vandana K Singh, David Mazaud, Manolis Fanto, David Chambers, Clive G Ballard, Joseph M Bateman

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Mitochondrial DNA Transport in Drosophila Neurons.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Article
  7. Review
  8. Mitochondrial retrograde signalling in neurological disease.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  9. Article
  10. Article
  11. Mitochondrial Involvement in Cisplatin Resistance.International journal of molecular sciences · 2019
    Review
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 2 institutions in 1 country.

Olivia F DuncanMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.
Lucy GranatMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.
Ramya RanganathanMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.
Vandana K SinghMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.
David MazaudMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.ORCID 0000-0003-3998-9330
Manolis FantoMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.ORCID 0000-0001-7807-2563
David ChambersWolfson Centre for Age-Related Diseases, King's College London, London, United Kingdom.
Clive G BallardMedical School Building, St Luke's Campus, University of Exeter, Exeter, United Kingdom.ORCID 0000-0003-0022-5632
Joseph M BatemanMaurice Wohl Clinical Neuroscience Institute, King's College London, London, United Kingdom.ORCID 0000-0003-0754-1785
King's College London · GBUniversity of Exeter · GB

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
NIH HHS P40 OD018537
6 · The paper itself

Abstract

Mitochondrial dysfunction activates the mitochondrial retrograde signaling pathway, resulting in large scale changes in gene expression. Mitochondrial retrograde signaling in neurons is poorly understood and whether retrograde signaling contributes to cellular dysfunction or is protective is unknown. We show that inhibition of Ras-ERK-ETS signaling partially reverses the retrograde transcriptional response to alleviate neuronal mitochondrial dysfunction. We have developed a novel genetic screen to identify genes that modify mitochondrial dysfunction in Drosophila. Knock-down of one of the genes identified in this screen, the Ras-ERK-ETS pathway transcription factor Aop, alleviates the damaging effects of mitochondrial dysfunction in the nervous system. Inhibition of Ras-ERK-ETS signaling also restores function in Drosophila models of human diseases associated with mitochondrial dysfunction. Importantly, Ras-ERK-ETS pathway inhibition partially reverses the mitochondrial retrograde transcriptional response. Therefore, mitochondrial retrograde signaling likely contributes to neuronal dysfunction through mis-regulation of gene expression.

Indexed as

AnimalsAnimals, Genetically ModifiedBehavior, AnimalDisease Models, AnimalDrosophilaDrosophila ProteinsExtracellular Signal-Regulated MAP KinasesEye ProteinsFemaleGene Expression ProfilingGene Expression RegulationGene Knockdown TechniquesHumansLeigh DiseaseMaleMitochondriaAOP protein, DrosophilaDrosophila ProteinsExtracellular Signal-Regulated MAP KinasesEye ProteinsMitochondrial Proteinspark protein, DrosophilaProto-Oncogene Proteins c-etsras ProteinsRepressor ProteinsSurf1 protein, DrosophilaUbiquitin-Protein Ligases

Identifiers

PMID30059502
PMCPMC6085068
OpenAlexW2883422710

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.