FB2024_03 , released June 25, 2024
Allele: Dmel\Arr23
Open Close
General Information
Symbol
Dmel\Arr23
Species
D. melanogaster
Name
FlyBase ID
FBal0042402
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Nucleotide substitution: T362A. Amino acid replacement: V52D.

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

T8648671A

Reported nucleotide change:

T362A

Amino acid change:

V52D | Arr2-PA

Reported amino acid change:

V52D

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

The visual pigment content of Arr23 flies is about 75% of wild-type.

Mutants show photoreceptor degeneration.

Partial impairment of trplninaE.T:Avic\GFP-EGFP translocation is observed in Arr23 mutant photoreceptors.

Mutant rhabdomeres degenerate. This phenotype is enhanced if the flies are fed sphingosine. Electroretinograms of 7 day old mutant flies exposed to light have a very small amplitude and slow inactivation kinetics.

Electroantennogram amplitudes in response to butanol or ethyl acetate are wild-type in Arr23 mutant flies.

Arr23 heterozygotes undergo retinal degeneration in room light in 8-10 days.

Photoreceptors show continuous quantum bump activity even in the absence of light stimulation.

Mutants exhibit a prolonged afterpotential (PDA) defect.

Mutant photoreceptors readily enter a prolonged depolarised afterpotential (PDA) upon blue light stimulation. Double mutants with CdsA1 are unable to enter or maintain a PDA, even after successive or prolonged blue light stimulation.

Whole cell voltage clamp recording of the light activated response of mutant photoreceptor cells show a large decrease in the rate of deactivation (defined as the recovery of the photoresponse after termination of the stimulus). Mutant photoreceptors undergo a prolonged depolarising afterpotential (DPA) with 10 times less photoconversion of rhodopsin to metarhodopsin than observed in wild type. Photoreceptors exhibit dramatic cellular degeneration 5 days after exposure to a 12 hour light-12 hour dark growth cycle. A mutation of norpA protects homozygous flies from light-activated retinal degradation.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressed by
Statement
Reference
Suppressor of
Statement
Reference

Arr23 is a suppressor of increased cell death phenotype of Arr11

Other
Statement
Reference
Phenotype Manifest In
Enhanced by
Statement
Reference

Arr23 has eye photoreceptor cell phenotype, enhanceable by Arr11

Arr23 has phenotype, enhanceable by Arr11

Suppressed by
Statement
Reference

Arr23 has rhabdomere phenotype, suppressible by lace[+]/lacek05305

Arr23 has ommatidium phenotype, suppressible by Gαq1

Suppressor of
Statement
Reference

Arr23 is a suppressor of eye photoreceptor cell phenotype of Arr11

Arr23 is a suppressor of rhabdomere phenotype of Arr11

Arr23 is a suppressor of ommatidium phenotype of Gαq1, rdgC306

Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The photoreceptor degeneration phenotype seen in Fatpk10307 clones in the retina is suppressed if the retinas are also mutant for Arr23.

The photoreceptor degeneration seen in Arr23 mutants is suppressed by expression of CDaseScer\UAS.cAa under the control of Scer\GAL4unspecified in the fat body.

trplninaE.T:Avic\GFP-EGFP translocation is severely inhibited in Arr11; Arr23 double mutant photoreceptors. trplninaE.T:Avic\GFP-EGFP is observed in the rhabdomeres of bouth light- and dark-raised flies.

Unlike Arr11 single mutants, Arr11;Arr23 flies show no photoreceptor degeneration.

Expression of CDaseScer\UAS.cAa under the control of Scer\GAL4GMR.PF suppresses rhabdomere degeneration in Arr23 flies and results in ommatidia that are similar to those of wild-type flies. Arr23 flies expressing CDaseScer\UAS.cAa under the control of Scer\GAL4GMR.PF have an electroretinogram with a large amplitude response, but the slow inactivation kinetics seen in Arr23 flies are not rescued. One copy of lacek05305 partially suppresses the degeneration of rhabdomeres seen in Arr23 flies; the rhabdomeres are mostly intact in the rescued flies, but some cellular degeneration (characterised by vacuoles and dark multivesicular bodies) is still seen.

Electroantennogram amplitudes in response to butanol or ethyl acetate are significantly reduced compared in Arr23; Arr12 double mutants compared to a control strain or two single mutants for either of these genes.

Gα49B1, Arr23 animals raised in normal light show normal ommatidial structure. The addition of Arr23 to rdgC306, Gα49B1 flies partially suppresses the Deep Pseudopupil seen in these flies.

Arr11; Arr23 double mutants exhibit a more severe decrease in rate of deactivation. Double mutants with ninaA8 and ninaAdelT,F can trigger and support strong PDAs.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments

Homozygote mutant phenotype can be fully rescued by P{Arr2+} restoring wild type visual physiology. Flies carrying a copy of P{Arr2+} have morphologically normal photoreceptor cells.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
References (25)