Nucleotide substitution: T362A. Amino acid replacement: V52D.
T8648671A
T362A
V52D | Arr2-PA
V52D
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.
Arr23 has abnormal neurophysiology phenotype, suppressible by CDaseUAS.cAa/Scer\GAL4GMR.PF
Arr23 is a suppressor of increased cell death phenotype of Arr11
Arr12, Arr23 has abnormal smell perception phenotype
Arr23 has eye photoreceptor cell phenotype, enhanceable by Arr11
Arr23 has eye photoreceptor cell phenotype, suppressible by Scer\GAL4unspecified/CDaseUAS.cAa
Arr23 has rhabdomere phenotype, suppressible by CDaseUAS.cAa/Scer\GAL4GMR.PF
Arr23 has rhabdomere phenotype, suppressible by lace[+]/lacek05305
Arr23 has ommatidium phenotype, suppressible by Gαq1
Arr23 is a suppressor of eye photoreceptor cell | somatic clone | cell autonomous | adult stage | conditional phenotype of Fatp1k10307
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
Arr11, Arr23 has eye photoreceptor cell phenotype
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.
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.
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.