FB2024_03 , released June 25, 2024
Allele: Dmel\α-Cat::shgshg.ΔCyt.UASp
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General Information
Symbol
Dmel\α-Cat::shgshg.ΔCyt.UASp
Species
D. melanogaster
Name
FlyBase ID
FBal0291803
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

Full-length α-Cat is fused to shg directly after the transmembrane domain of shg (at bp 4746). The cytoplasmic domain of shg is absent. The construct is cloned downstream of UASp regulatory 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 ( 0 )
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

Expression of shg::α-Catshg.ΔCyt.Scer\UAS under the control of Scer\GAL4Scer\FRT.Rnor\CD2.αTub84B gives rise to very mild migration defects.

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

The co-expression of α-Cat::shgshg.ΔCyt.UASp does not suppress the ionizing radiation-induced basal cell delamination in the wing disc posterior compartment observed in individuals expressing BacA\p35UAS.cHa under the control of Scer\GAL4en.PU.

Expression of shg::α-Catshg.ΔCyt.Scer\UAS in follicle cells using the MARCM system and Scer\GAL4Scer\FRT.Rnor\CD2.αTub84B fails to suppress the follicle cell sorting, loss of epithelial integrity and oocyte mispositioning phenotypes seen in shgR69/+ mutant follicle cell clones.

Expression of shg::α-Catshg.ΔCyt.Scer\UAS in wild-type egg chambers using the MARCM system and Scer\GAL4Scer\FRT.Rnor\CD2.αTub84B leads to a very mild cell migration defect. In mixed border cell clusters, in which half of the cells are wild-type and the other half are shgR69 mutant cells expressing shg::α-Catshg.ΔCyt.Scer\UAS, mild delays in migration are seen. This is similar to the phenotype seen in border cells that are half wild-type and half shgR69 mutant. Interestingly, in the presence of shg::α-Catshg.ΔCyt.Scer\UAS, mixed shgR69/wild-type border cell clusters are never split, and all possible ratios of wild-type to mutant cells are observed.

Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
shg::α-Catshg.ΔCyt.Scer\UAS.P\T
shg::α-Catshg.ΔCyt.Scer\UAS
α-Cat::shgshg.ΔCyt.Scer\UAS.P\T
α-Cat::shgshg.ΔCyt.UASp
Name Synonyms
Secondary FlyBase IDs
    References (3)