Flies expressing WASpH242D.Scer\UAS under the control of Scer\GAL4arm.PS in a WASp1/Df(3R)3450 mutant background display similarly elongated cysts to wild type, but no sperm is released into the seminal vesicle. Coiling of the cysts does not take place, and the extreme basal end of the testis tube, lined by the terminal epithelium and leading up to the seminal vesicle, is free of cysts altogether. Sperm individualisation in these mutants proceeds normally. The microfilaments and nuclei of late-stage cysts show significant structural alterations. There is a consistent failure to achieve the intertwined and tightly packed organisation of head cyst cell F-actin arrays and associated spermatid nuclei. The microfilament arrays appear sparse and misshapen, and the normally tight and uniformly oriented bundles of nuclei are loosely packed and partially split.
Expression of WASpH242D.Scer\UAS under the control of Scer\GAL4n-syb.PS rescues the neuromuscular junction overgrowth seen in WASp1/Df(3R)3450 third instar larvae.
The addition of WASpH242D.Scer\UAS driven by Scer\GAL4arm.PS to WASp1/Df(3R)3450 flies, rescues the bristle phenotype seen in these animals.