Evidence map›Paper›PMID 25313867›Full record

ArticleeLife2014

Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production.

Hector Sandoval, Chi-Kuang Yao, Kuchuan Chen, Manish Jaiswal, Taraka Donti, Yong Qi Lin, Vafa Bayat, Bo Xiong, Ke Zhang, Gabriela David and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

79 citing papers in PubMed, 151 citations in OpenAlex.

  1. Mitochondrial CaBiomolecules · 2026
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19 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

15 authors at 3 institutions in 1 country.

Hector SandovalDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Chi-Kuang YaoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Kuchuan ChenProgram in Developmental Biology, Baylor College of Medicine, Houston, United States.
Manish JaiswalDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Taraka DontiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Yong Qi LinHoward Hughes Medical Institute, Baylor College of Medicine, Houston, United States.
Vafa BayatProgram in Developmental Biology, Baylor College of Medicine, Houston, United States.
Bo XiongProgram in Developmental Biology, Baylor College of Medicine, Houston, United States.
Ke ZhangProgram in Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, Houston, United States.
Gabriela DavidProgram in Developmental Biology, Baylor College of Medicine, Houston, United States.
Wu-Lin CharngDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Shinya YamamotoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Lita DuraineHoward Hughes Medical Institute, Baylor College of Medicine, Houston, United States.
Brett H GrahamDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Hugo J BellenDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
Baylor College of Medicine · USHoward Hughes Medical Institute · USNeurological Research Institute · US

Funding

UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI PAYLOR, RICHARD E · 1988 to 2013
$29.4M
Transposon induced disruption of most Drosophila genesR01GM067858 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2003 to 2020
$15.7M
Research Education and Career Horizons ProgramK12GM084897 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SIFERS, RICHARD NORMAN, SLAUGHTER, GAYLE · 2008 to 2016
$8.3M
Steps towards a paternal gene activation therapy for Angelman syndromeU54HD083092 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI NELSON, DAVID LOREN, NEUL, JEFFREY L · 2014 to 2019
$7.8M
Mutidisciplinary Training;Brain Disorders &DevelopmentT32NS043124 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI SWANN, JOHN WILLIAM · 2002 to 2021
$4.6M
Mapping and rescuing EMS-induced lethal mutations on the Drosophila X ChromosomeRC4GM096355 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2010 to 2010
$1.7M
Succinyl-COA Synthetase Deficiency: A Model to Study Mitochondrial DNA (MTDNA) DeR01GM098387 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI GRAHAM, BRETT HARRISON · 2012 to 2016
$1.5M
Developmental Biology Training ProgramT32HD055200 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2007 to 2011
$1.3M
NICHD NIH HHS P30 HD024064NICHD NIH HHS T32 HD055200NICHD NIH HHS U54 HD083092NIGMS NIH HHS K12 GM084897NIGMS NIH HHS R01 GM067858NIGMS NIH HHS R01 GM098387NIGMS NIH HHS RC4 GM096355NIGMS NIH HHS RC4GM096355-01NINDS NIH HHS T32 NS043124
6 · The paper itself

Abstract

Mitochondrial fusion and fission affect the distribution and quality control of mitochondria. We show that Marf (Mitochondrial associated regulatory factor), is required for mitochondrial fusion and transport in long axons. Moreover, loss of Marf leads to a severe depletion of mitochondria in neuromuscular junctions (NMJs). Marf mutants also fail to maintain proper synaptic transmission at NMJs upon repetitive stimulation, similar to Drp1 fission mutants. However, unlike Drp1, loss of Marf leads to NMJ morphology defects and extended larval lifespan. Marf is required to form contacts between the endoplasmic reticulum and/or lipid droplets (LDs) and for proper storage of cholesterol and ecdysone synthesis in ring glands. Interestingly, human Mitofusin-2 rescues the loss of LD but both Mitofusin-1 and Mitofusin-2 are required for steroid-hormone synthesis. Our data show that Marf and Mitofusins share an evolutionarily conserved role in mitochondrial transport, cholesterol ester storage and steroid-hormone synthesis.

Indexed as

AnimalsAnimals, Genetically ModifiedAxonsCholesterolCytoskeletal ProteinsDrosophila melanogasterDrosophila ProteinsEcdysoneEndoplasmic ReticulumGene Expression Regulation, DevelopmentalGenetic Complementation TestGTP-Binding ProteinsGTP PhosphohydrolasesHumansLarvaLipid DropletsCholesterolCytoskeletal ProteinsDrosophila ProteinsDRP1 protein, DrosophilaEcdysoneGTP-Binding ProteinsGTP PhosphohydrolasesMarf protein, DrosophilaMembrane ProteinsMfn1 protein, humanMFN2 protein, humanMiro protein, DrosophilaMitochondrial Membrane Transport ProteinsMitochondrial Proteinsrho GTP-Binding ProteinsCharcot-Marie-Tooth type 2Adevelopmental biologydrosophila melanogasterDrp1endoplasmic reticulumlipid dropletsMfn1 and Mfn2mitochondria transportneuroscienceOpa1stem cells

Identifiers

PMID25313867
PMCPMC4215535
OpenAlexW2105186030

What OpenQuestion holds

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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.