FB2024_03 , released June 25, 2024
Allele: Dmel\dshΔDEP+.UAS
Open Close
General Information
Symbol
Dmel\dshΔDEP+.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0093072
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-dshΔDEP
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

dsh amino acids 1 to 394 are expressed under the control of UASt 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

Expressing dshΔDEP+.UAS under the control of Scer\GAL4HCH.Hand fails to induce defects in heart morphology or ostia formation in embryos.

Expression of dshΔDEP+.Scer\UAS under the control of Scer\GAL4fkh.PZ has no effect on salivary gland guidance in the embryo.

Expression of the dominant-negative dshΔDEP+.Scer\UAS in the retina behind the furrow using Scer\GAL4GMR.PF results in a strong ventral-to-dorsal R axon misrouting phenotype.

Expression of dshΔDEP+.Scer\UAS under the control of Scer\GAL4ptc-559.1 results in a polarity defect.

Expression of dshΔDEP+.Scer\UAS at 24 hours after pupariation under the control of Scer\GAL4hs.PB results in a tissue polarity phenotype in the wing.

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

dshΔDEP+.Scer\UAS; Scer\GAL4da.G32 partially suppresses the transformation of naked ventral cuticle into denticles and reduction in cuticle length seen in cuticles from wgl-17 homozygous embryos, and an completely suppress the dorsal hole in these cuticles. dshΔDEP+.Scer\UAS; Scer\GAL4da.G32 suppresses, the loss of dorsal ventral polarity in the leading edge cells of stage 13 wgl-17 homozygous embryos but fails to rescue elongation of these cells. However, initiation of the anterior zipper during dorsal closure is rescued.

The dorsal hole phenotype, loss of leading edge actin cable, and loss of adhesion between the amnioserosa and dorsal epidermis of hep1 mutant embryos are all partially suppressed by Scer\GAL469B with dshΔDEP+.Scer\UAS.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to rescue
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
dshΔDEP+.Scer\UAS
dshΔDEP+.UAS
Name Synonyms
Secondary FlyBase IDs
    References (9)