FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\PRKNWT.UAS
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General Information
Symbol
Hsap\PRKNWT.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0287974
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulates expression of wild type Hsap\PRKN cDNA.

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 ( 0 )
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

Scer\GAL4elav.PU-mediated expression of Hsap\PARK2WT.Scer\UAS does not compromise the overall anatomical integrity of the adult brain.

PPL1 and PAM (as well as PAL, PPL2, PPM1/2 and PPM3) neurons remain intact in flies expressing Hsap\PARK2WT.Scer\UAS via Scer\GAL4Ddc.PL.

Scer\GAL4elav.PU, Hsap\PARK2WT.Scer\UAS fly brains do not exhibit loss of dopaminergic PPL1 neurons or serotonergic neurons.

Scer\GAL4Ddc.PL, Hsap\PARK2WT.Scer\UAS flies do not show a significant impairment in the ability in their climbing ability compared to controls.

The morphology of surviving PPL1 neurons in Scer\GAL4Ddc.PL, Hsap\PARK2WT.Scer\UAS flies exposed to rotenone is relatively uncompromised compared to controls. The number of PPL1, PPL2 and PAM neurons in Scer\GAL4Ddc.PL, Hsap\PARK2WT.Scer\UAS flies exposed to rotenone is considerably increased compared to controls. The climbing ability of Scer\GAL4Ddc.PL, Hsap\PARK2WT.Scer\UAS flies exposed to rotenone is considerably increased compared to controls.

The indirect flight muscles of Scer\GAL4how-24B, Hsap\PARK2WT.Scer\UAS flies do not show abnormal mitochondria - mitochondria are generally intact.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference

Expression of Hsap\PARK2WT.Scer\UAS suppresses the mitochondrial defects seen in the flight muscles when Hsap\LRRK2G2019S.Scer\UAS.T:Hsap\MYC is expressed under the control of Scer\GAL4how-24B. The climbing defects are also rescued.

Expression of Hsap\PARK2WT.Scer\UAS suppresses the mitochondrial defects seen in dopaminergic neurons when Hsap\LRRK2G2019S.Scer\UAS.T:Hsap\MYC is expressed under the control of Scer\GAL4Ddc.PL.

The accelerated loss of DA neurons in the PPM 2/3 clusters of rotenone-treated flies expressing Hsap\LRRK2G2019S.Scer\UAS.T:Hsap\MYC via Scer\GAL4Ddc.PL is mitigated through co-expression of Hsap\PARK2WT.Scer\UAS.

The significant degeneration of DA neurons in the PPM clusters 1 and 3 in 60 day old flies expressing Hsap\LRRK2G2019S.Scer\UAS.T:Hsap\MYC via Scer\GAL4Ddc.PL is mitigated through co-expression of Hsap\PARK2WT.Scer\UAS.

Scer\GAL4Ddc.PL-mediated expression of Hsap\PARK2WT.Scer\UAS significantly protects against the degeneration of PPL1 and PAM dopaminergic neurons normally seen in 20-day old park1 flies.

The mitochondrial defects seen in park1 indirect flight muscles are significantly mitigated by Scer\GAL4how-24B-mediated expression of Hsap\PARK2WT.Scer\UAS.

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
Hsap\PARK2WT.Scer\UAS
Hsap\PRKNWT.Scer\UAS
Hsap\PRKNWT.UAS
Name Synonyms
Secondary FlyBase IDs
    References (4)