FB2026_02 , released June 18, 2026
Allele: Dmel\auxKK100927
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General Information
Symbol
Dmel\auxKK100927
Species
D. melanogaster
Name
FlyBase ID
FBal0230996
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulatory sequences drive expression of an inverted repeat.

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 )
Disease
Interaction
References
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 auxKK100927 (together with UAS-Dicer2 to enhance RNAi efficiency) under the control of either Scer\GAL4ple.PU or Scer\GAL4Ddc.PU leads to age-progressive decline of the adult locomotor (climbing) abilities. Scer\GAL4ple.PU-driven expression also results in age-dependent loss of dopaminergic neurons from the PPM1/2 in the brain of aged (33 days old) but not young (3 days old) adult flies. Expression driven by the Scer\GAL4GMR58E02 driver has no evident effect on the number of dopaminergic neurons from the PAM cluster regardless of age.

External Data
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference

The loss of dopaminergic PPM1/2 neurons observed even in very young adult flies expressing Hsap\SNCAA30P.Scer\UAS.cUa under the control of Scer\GAL4Ddc.PU is exacerbated further by co-expression of auxKK100927 RNAi and the number of neurons is further decreased. Simultaneous expression of the two transgenes driven by Scer\GAL4ple.PU also leads to early-onset loss of PPM1/2, which is otherwise not observed in young (3 or 10 days old) flies expressing either of the transgenes alone with this driver.

Complementation and Rescue Data
Comments

The age-progressive rapid deterioration in adult locomotion (climbing ability) characteristic for flies expressing auxKK100927 (together with UAS-Dicer2 to enhance RNAi efficiency) under the control of either Scer\GAL4ple.PU or Scer\GAL4Ddc.PU can be rescued by co-expression of auxFL.Scer\UAS.T:Avic\GFP.

Co-expression of Hsap\SNCAScer\UAS.cUa (but not Hsap\SNCAA53T.Scer\UAS.cUa) with auxKK100927 leads to significant decrease in the number of dopaminergic PPM1/2 neurons in the brains of young (3 and/or 10 days old) adult flies, which is not observed at this age when any of the transgenes is expressed alone.

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Mutant
Wild-type
Stocks (1)
Notes on Origin
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
auxKK100927
auxR103426
Name Synonyms
Secondary FlyBase IDs
    References (3)