FB2025_01 , released February 20, 2025
Allele: Dmel\DAAMC.UASp
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General Information
Symbol
Dmel\DAAMC.UASp
Species
D. melanogaster
Name
FlyBase ID
FBal0314316
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-C-DAAM
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASp regulatory sequences drive expression of amino acids 518-1153 of DAAM. This is produces an activated form of DAAM.

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 DAAMC.Scer\UAS.P\T under the control of Scer\GAL4ey-OK107 induces very severe growth and guidance defects in the mushroom body axons Unlike in wild type, these axons fail to project anteriorly and form a huge, unstructured, randomly oriented network of projections with very prominent but misprojected bundles in the posterior region of the brain.

Expression of DAAMC.Scer\UAS.P\T pan-neuronally, under the control of Scer\GAL4elav-C155, results in severe fasciculation defects and embryonic lethality. The majority of embryos (78%) display a more prominent neuropile than observed in wild-type, commissures and nerve roots in particular appear thicker. Many axons are misrouted, and either cross the midline or exit the bundles into lateral directions.

Expression of DAAMC.Scer\UAS.P\T in the trachea, driven by Scer\GAL4btl.PS, causes distinct phenotypic effects in the fusion cells and the regular tracheal cells. In fusion cells of this genotype, there is a dramatic change in the actin organization and cuticle pattern, causing strong actin accumulation at the apical surface. The typical granular cuticle pattern is transformed towards a stripy pattern , partly resembling the taenidial folds of normal tracheal cells. Most of the actin in these cells is found in largely unorganized bundles. In tracheal cells, DAAMC.Scer\UAS.P\T overexpression results in severe impairment of taenidial fold formation and actin organization.

Coexpression of DAAMScer\UAS.P\T.cMa and DAAMC.Scer\UAS.P\T, under the control of Scer\GAL4btl.PS, causes a suppression of the Scer\GAL4btl.PS/DAAMC.Scer\UAS.P\T phenotype in regular tracheal cells but not in fusion cells.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT Enhanced by
Suppressed by
Statement
Reference

DAAMC.UASp has abnormal neuroanatomy phenotype, suppressible by ena23/ena[+]

DAAMC.UASp has abnormal neuroanatomy phenotype, suppressible by ena[+]/enaGC1

NOT suppressed by
Statement
Reference

DAAMC.UASp, Scer\GAL4ey-OK107 has abnormal neuroanatomy phenotype, non-suppressible by dsh1/dsh[+]

Phenotype Manifest In
NOT Enhanced by
Statement
Reference
Suppressed by
NOT suppressed by
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

dsh1 does not suppress the growth and guidance defects seen in the mushroom body axons of flies expressing DAAMC.Scer\UAS.P\T under the control of Scer\GAL4ey-OK107.

The Scer\GAL4elav-C155/DAAMC.Scer\UAS.P\T gain-of-function phenotype (i.e the appearance of thicker commissures and nerve roots) is not affected by Rac1 gene dose (i.e. a Rac1J11/+ or Rac1J11/Rac1J10 background), a Rac1J11, Rac2Δ background or a Rac1J10, Rac2Δ, MtlΔ background.

The Scer\GAL4elav-C155/DAAMC.Scer\UAS.P\T gain-of-function phenotype (i.e the appearance of thicker commissures and nerve roots) is not affected by a chic221/+ background.

The Scer\GAL4elav-C155/DAAMC.Scer\UAS.P\T gain-of-function phenotype (i.e the appearance of thicker commissures and nerve roots) is suppressed by a ena23/+ or enaGC1/+ background.

The tracheal cuticle defects of larvae that express DAAMC.Scer\UAS.P\T under the control of Scer\GAL4btl.PS are dominantly suppressed by Src42AE1 and Btk29Ak05610. However, Rho172F does not modify the effect of modify the effect of DAAMC.Scer\UAS.P\T expression.

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
DAAMC.Scer\UAS.P\T
DAAMC.UASp
DAAMCA.Scer\UAS
Name Synonyms
Secondary FlyBase IDs
  • FBal0194065
  • FBal0240537
References (7)