FB2024_03 , released June 25, 2024
Allele: Dmel\stac3B20
Open Close
General Information
Symbol
Dmel\stac3B20
Species
D. melanogaster
Name
FlyBase ID
FBal0320014
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

T to A mutation in the 5' splice site of the last intron, resulting in intron retention and the introduction of a stop codon five nucleotides after the mutated splice site. This is predicted to result in a truncated protein lacking the C-terminal 30 amino acids of the wild-type product.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

T25064118A

Reported nucleotide change:

T?A

Comment:

T to A mutation in the 5' splice site of the last intron, resulting in intron retention and the introduction of a stop codon five nucleotides after the mutated splice site. This is predicted to result in a truncated protein lacking the C-terminal 30 amino acids of the wild-type product.

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

stac3B20/stac3B20 mutant embryos display interruptions in the dorsal trunk tracheal lumen, but not the tracheal epithelium, at points where tracheal tip cells normally meet to form anastomoses. The fusion cells are properly specified, and migrate, connect, polarize, and expand apical membrane domains and lumen, but fail to fuse their apical domains.

The presence of a single stac3B20/stac3B20 fusion cell in stac3B20/+ embryos leads to a tracheal luminal fusion defect.

stac3B20/Df(3R)BSC493 mutant embryos display defects in dorsal branch tube fusion.

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

Expression of dndScer\UAS.cKa, Rab7Scer\UAS.P\T.T:Avic\GFP-YFP or Rab39Scer\UAS.P\T.T:Avic\GFP-YFP under the control of Scer\GAL4dysf.C1.7 fails to rescue the tracheal fusion defects of stac3B20/stac3B20 mutant embryos.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of stacT:Scer\TY1,T:Zzzz\TEV.CS,T:Avic\GFP-SF,T:Zzzz\FLAG, or stacScer\UAS.B.T:Avic\GFP-EGFP under the control of Scer\GAL4dysf.C1.7, but not stac3B20.Scer\UAS.A.T:Avic\GFP-EGFP under the control of Scer\GAL4dysf.C1.7, in embryos partially rescues the tracheal defects of stac3B20/stac3B20 embryos.

Expression of stacScer\UAS.A.T:Avic\GFP-EGFP under the control of Scer\GAL4dysf.C1.7 partially rescues, or under the control of Scer\GAL4btl.PU fully rescues the tracheal defects of stac3B20/stac3B20 embryos.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)