Amino acid replacement: W641term.
G30465308A
G?A
W641term | CDase-PA; W641term | CDase-PB; W641term | CDase-PC; W641term | CDase-PD; W641term | CDase-PE; W641term | CDase-PF
W641term
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.
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.
CDase1 has lethal | recessive phenotype, suppressible by Scer\GAL4Act.PU/bwaUAS.cYa
CDase1 has eye photoreceptor cell phenotype, suppressible by BacA\p35GMR.PH
Overexpression of bwaScer\UAS.cYa driven by Scer\GAL4Act.PU suppresses the lethality of CDase1.
Expression of BacA\p35GMR.PH suppresses the light-induced retinal degeneration that is seen in CDase1 flies.