FB2025_01 , released February 20, 2025
Allele: Dmel\CDase1
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General Information
Symbol
Dmel\CDase1
Species
D. melanogaster
Name
FlyBase ID
FBal0241853
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: W641term.

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

G30465308A

Reported nucleotide change:

G?A

Amino acid change:

W641term | CDase-PA; W641term | CDase-PB; W641term | CDase-PC; W641term | CDase-PD; W641term | CDase-PE; W641term | CDase-PF

Reported amino acid change:

W641term

Comment:

G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase base on reported amino acid change.

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

CDase1 is homozygous and hemizygous lethal.

Animals in which almost the entire eye is homozygous (generated using the eyFLP system) have a normal rhabdomere architecture at 15 days after eclosion.

Hemizygous CDase1 adult escapers (which survive due to the presence of a closely linked suppressor mutation on the same chromosome that suppresses some of the lethality caused by CDase1) show severe photoreceptor degeneration 5 days after eclosion when they are raised in regular light and dark cycles. Many photoreceptor cells are missing their rhabdomeres and have vacuolated cell bodies. This photoreceptor degeneration is not suppressed by feeding with sphingosine. 5 day old mutant flies raised in constant darkness do not show photoreceptor degeneration, however they do not show an electroretinogram response (even to high-intensity light).

Mutant third instar larvae show increased apoptosis in eye imaginal discs, mostly anterior to the morphogenetic furrow, compared to control larvae. The imaginal discs of irradiated mutant third instar larvae show higher levels of apoptosis than those of irradiated control larvae.

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

Overexpression of bwaScer\UAS.cYa driven by Scer\GAL4Act.PU suppresses the lethality of CDase1.

Xenogenetic Interactions
Statement
Reference

Expression of BacA\p35GMR.PH suppresses the light-induced retinal degeneration that is seen in CDase1 flies.

Complementation and Rescue Data
Rescued by
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
Name Synonyms
Secondary FlyBase IDs
    References (2)