Point mutation (G to A) in the splice donor site after the fourth exon. This results in the retention of a 26bp intron fragment, causing a frameshift that produces an in-frame stop codon immediately following the mutated donor site (the amino acid residue prior to the stop codon is also changed from Phe to Leu).
G19400004A
G?A
Mutation in splice donor for fourth intron of Ino80
sterile (with Df(3R)ED5942)
Most homozygous and Ino80psg25/Df(3R)ED5942 animals die after head eversion, either as pupae or pharate adults. Approximately 15% of animals eclose, but they are sterile. Arrested mutant pupae and pharate adults appear morphologically normal.
Ino80psg25/Df(3R)ED5942 animals have a persistant salivary gland phenotype (85.2% penetrance) at 24 hours after puparium formation (APF). Caspase activation appears to be delayed in the mutant salivary glands compared to wild type.
Ino80psg25/Df(3R)ED5942 animals show a 2 hour delay in the timing of head eversion compared to controls. Those animals that eclose do so approximately one day later than controls.
Ino80psg25/Df(3R)ED5942 has abnormal developmental rate phenotype, suppressible | heat sensitive by ftz-f1hs.PW
Expression of ftz-f1hs.PW is induced by a heat shock at 7 hours after puparium formation rescues the timing of head eversion in Ino80psg25/Df(3R)ED5942 animals to normal.
Ino80psg25/Df(3R)ED5942 is rescued by Ino80hs.PN
Ino80psg25 is rescued by Ino80hs.PN
Leaky expression of Ino80hs.PN is able to rescue both the lethality and sterility observed in homozygous Ino80psg25 and Ino80psg25/Df(3R)ED5942 animals. In addition, the developmental delay seen in Ino80psg25/Df(3R)ED5942 animals is also rescued.