FB2024_03 , released June 25, 2024
Allele: Dmel\FrlDN.UAS
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General Information
Symbol
Dmel\FrlDN.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0318783
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulates expression of dominant negative (DN) Frl through deletion of the FH2 domain and C terminus (ΔFH2).

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 FrlDN.Scer\UAS driven by Scer\GAL4hs.2sev causes a severe rough eye phenotype; when driven by Scer\GAL4sev.EP there are ommatidial rotation defects (planar cell polarity-like defects) in adult eyes, along with the loss of R-cell clusters (co-expression of FrlCA.Scer\UAS does not alter the phenotype). Third instar larvae with expression of FrlDN.Scer\UAS driven by Scer\GAL4sev.EP have misrotated ommatidial clusters and clusters lacking R-cells in eye discs.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
NOT Enhanced by
Suppressed by
Enhancer of
Suppressor of
Phenotype Manifest In
Enhanced by
NOT Enhanced by
Statement
Reference

FrlDN.UAS, Scer\GAL4sev.EP has ommatidium phenotype, non-enhanceable by nmoP1

FrlDN.UAS, Scer\GAL4sev.EP has ommatidium phenotype, non-enhanceable by shg1

FrlDN.UAS, Scer\GAL4sev.EP has ommatidium phenotype, non-enhanceable by nmoDB

Suppressed by
Enhancer of
Suppressor of
Additional Comments
Genetic Interactions
Statement
Reference

R-cell loss in flies with Cdc42Scer\UAS.cWa driven by Scer\GAL4sev.EP is completely suppressible with co-expression of FrlDN.Scer\UAS.

Co-expression of Cdc42Scer\UAS.cWa suppresses the ommatidial rotation phenotypes (planar cell polarity-like defects) seen in flies with FrlDN.Scer\UAS driven by Scer\GAL4sev.EP. Presence of Cdc421/+ enhances the ommatidial rotation phenotypes and increases R-cell loss seen eyes of in flies with FrlDN.Scer\UAS driven by Scer\GAL4sev.EP.

Expression of FrlDN.Scer\UAS driven by Scer\GAL4sev.EP enhances (likely additive) eye phenotypes (ommatidial rotation defects and R-cell loss) in flies with Rac1V12.Scer\UAS driven by Scer\GAL4hs.2sev.

Presence of shg1, shgk03401, nmoDB or nmoP1 does not significantly alter eye phenotypes seen in flies with FrlDN.Scer\UAS driven by Scer\GAL4sev.EP.

Presence of Df(2L)CadNΔ14/+ or Df(2L)BSC148/+ enhances ommatidial rotation (planar cell polarity-like defects) seen in flies with FrlDN.Scer\UAS driven by Scer\GAL4sev.EP.

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 (2)
Reported As
Symbol Synonym
FrlDN.Scer\UAS
FrlDN.UAS
Name Synonyms
Secondary FlyBase IDs
    References (1)