FB2024_03 , released June 25, 2024
Allele: Dmel\sqhDD.UAS
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General Information
Symbol
Dmel\sqhDD.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0263515
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-sqhDD, UAS-SqhD20D21
Key Links
Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulatory sequences drive expression of an activated form of sqh carrying amino acid substitutions T20E and S21E to mimic the constitutive phosphorylated form.

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 )
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

Cells from clones in the eye disc expressing sqhDD.Scer\UAS under the control of Scer\GAL4Act.PU become mislocalised in the optic stalk.

Cells from the eye disc expressing sqhDD.Scer\UAS under the control of Scer\GAL4ey.PU become mislocalised in the optic stalk.

Wing discs overexpressing sqhDD.Scer\UAS under the control of Scer\GAL4Bx-MS1096 are multi-layered and show malformed disc shapes.

In contrast to the columnar wild-type cells, wing disc cells in clones overexpressing sqhDD.Scer\UAS driven by Scer\GAL4Act5C.PI shrink basally and show abnormal apical-basal polarity.

In contrast to wild-type controls, cells overexpressing sqhDD.Scer\UAS under the control of Scer\GAL4ptc-559.1 appear to migrate out from the Scer\GAL4ptc-559.1-expression domain.

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

Co-expressing sqhDD.UAS enhances the larval brain glia hyperplasia induced by the expression of btl::Egfrλ.UAS under the control of Scer\GAL4repo.PU; glia cells lose the normal stellate shape and form abnormal cellular aggregates that disrupted normal larval brain architecture, indicative of neoplastic transformation.

The severity of the embryonic cuticle defects in α-Cat1 or α-Cat13 mutants but not in α-Cat421 or α-Cat2049 embryos can be significantly aggravated by expression of sqhDD.Scer\UAS under the control of Scer\GAL4c381 in the mutant background.

Co-expression of sqhDD.Scer\UAS with sqadsRNA.Scer\UAS under the control of Scer\GAL4Act5C.PP suppresses the sqadsRNA.Scer\UAS-induced autophagic defects in larval fat body cells.

Xenogenetic Interactions
Statement
Reference
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
sqhDD.Scer\UAS
sqhDD.UAS
Name Synonyms
Secondary FlyBase IDs
    References (10)