FB2024_03 , released June 25, 2024
Allele: Dmel\DysRNAi.RB.UAS
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General Information
Symbol
Dmel\DysRNAi.RB.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0244101
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UAS regulatory sequences drive expression of a hairpin loop which targets the short form of Dys (Dp186).

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 ( 0 )
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

Flies expressing DysdsRNA.RB.Scer\UAS under the control of Scer\GAL4tub or Scer\GAL4how-24B show comparable climbing ability at the beginning of adult life to control flies. However, the ability of these animals to climb declines significantly faster over time compared to controls. Animals expressing DysdsRNA.RB.Scer\UAS under the control of Scer\GAL4tub exhibit mostly normal muscle architecture at 3 days after eclosion. By 12 days, age-dependent muscle degeneration is observed including loss of muscle fibre organisation, vacuolisation and the absence of some muscles.

Expression of DysdsRNA.RB.Scer\UAS in the eye disc (under the control of Scer\GAL4GMR.PU), or in all glial cells (under the control of Scer\GAL4repo.PU), both result in photoreceptor axon targeting defects. Axons stop irregularly, making gaps in the normal termination zone of the lamina plexus, deviating from the path and bundling aberrantly. Expression of DysdsRNA.RB.Scer\UAS in the mesodermal tissue (under the control of Scer\GAL4how-24B) does not effect the axon termination process.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
DysRNAi.RB.UAS
DysdsRNA.RB.Scer\UAS
DysdsRNA.RB.UAS
Name Synonyms
Secondary FlyBase IDs
    References (2)