FB2026_03 , released September 17, 2026
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Citation
Sandoval, H., Yao, C.K., Chen, K., Jaiswal, M., Donti, T., Lin, Y.Q., Bayat, V., Xiong, B., Zhang, K., David, G., Charng, W.L., Yamamoto, S., Duraine, L., Graham, B.H., Bellen, H.J. (2014). Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production.  eLife 3(): e03558.
FlyBase ID
FBrf0226654
Publication Type
Research paper
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.
PubMed ID
PubMed Central ID
PMC4215535 (PMC) (EuropePMC)
Related Publication(s)
Personal communication to FlyBase

Location data for Marf alleles.
Sandoval, 2015.5.4, Location data for Marf alleles. [FBrf0228283]

Marf, Opa1 and Drp1 insertions.
Bellen, 2017.1.20, Marf, Opa1 and Drp1 insertions. [FBrf0234643]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    eLife
    Title
    eLife
    ISBN/ISSN
    2050-084X
    Data From Reference
    Aberrations (2)
    Alleles (19)
    Gene Groups (1)
    Genes (6)
    Human Disease Models (1)
    Natural transposons (1)
    Insertions (2)
    Experimental Tools (3)
    Transgenic Constructs (9)