FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\MiroUAS.cGa
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General Information
Symbol
Dmel\MiroUAS.cGa
Species
D. melanogaster
Name
FlyBase ID
FBal0239860
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-Miro, UAS-dMiro
Key Links
Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

Expression of Miro cDNA (longest splice form) is under the control of UAS sequences.

Allele components
Component
Use(s)
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 1 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 1 )
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Expression of MiroScer\UAS.cGa under the control of Scer\GAL4dpr1-PGaw strongly reduces the number of mitochondria that undergo axonal transport in both anterograde and retrograde directions in the wing marginal nerve, as compared to controls.

Expression of MiroScer\UAS.cGa under the control of Scer\GAL4ple.PF causes aberrant mitochondrial aggregation in dopaminergic neurons, and dopaminergic neuron loss, in adults.

Expression of MiroScer\UAS.cGa under the control of Scer\GAL4ple.PF in larval motor neurons results in decreased flux in axonal mitochondrial transport in both anterograde and retrograde directions, increased velocity of anterograde (but not retrograde) mitochondrial transport, increased mitochondrial length, and accumulation of mitochondria in the most distal boutons of neuromuscular junctions, as compared with controls.

MiroScer\UAS.cGa; Scer\GAL4elav-C155 larvae show excessive accumulation of mitochondria at the neuro-muscular junctions

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
NOT Enhanced by
NOT suppressed by
Enhancer of
Suppressor of
NOT Suppressor of
Other
Additional Comments
Genetic Interactions
Statement
Reference

Individuals co-expressing Hsap\TRPV4R269C.UAS.BID and MiroUAS.cGa frequently fail to expand their wings after eclosion.

Expression of MiroScer\UAS.cGa under the control of Scer\GAL4Mhc.PU enhances the abnormal wing posture and flight defects of Pink1B9/Pink1B9 mutants.

Expression of MiroScer\UAS.cGa under the control of Scer\GAL4ple.PF in a Pink1B9/Pink1B9 mutant background does not result in a significant difference in dopaminergic neuron number as compared to in a wild-type background, but does result in reduced viability.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescues
Fails to rescue
Comments

MiroScer\UAS.cGa; Scer\GAL4elav-C155 rescues most of the phenotypes due to MiroB682/MiroB682 : larval lethality, larval body and muscle size, distribution of mitochondria to the distal extremities of neurons, neuro-muscular junction morphology and microtubule cytoskeleton organization. However, distribution of mitochondria within somatic muscle is not rescued in these animals. None of the phenotypes rescued by MiroScer\UAS.cGa; Scer\GAL4elav-C155 are rescued by MiroScer\UAS.cGa; Scer\GAL4how-24B.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
MiroScer\UAS.cGa
MiroUAS.cGa
Name Synonyms
Secondary FlyBase IDs
    References (12)