85% of homozygous Dmtne01970 escapers exhibit wing expansion defects. No defects are seen in heterozygous controls.
Most homozygous Dmtne01970 mutant flies die during metamorphosis and adult escapers die within a few days. Heterozygotes have a normal lifespan. The optic lobes of homozygous but not heterozygous Dmtne01970 flies are severely reduced in size, and missing much of the medulla neuropil.
10 day old Dmtne01970 mutant flies in which Dmtn expression has been rescued in glia (through expression of DmtnScer\UAS.cHa under the control of Scer\GAL4repo) show evidence of neurodegeneration in the form of vacuoles. These vacuoles are rarely seen in 10 day old flies expressing DmtnScer\UAS.cHa in neurons under the control of Scer\GAL4elav-C155, or expressing DmtnScer\UAS.cHa in both neurons and glia. Vacuoles are not seen in any of the rescued flies at one day old.
Dmtne01970 mutant flies expressing DmtnScer\UAS.cHa in glia under the control of Scer\GAL4repo have a severely reduced lifespan compared to those expressing DmtnScer\UAS.cHa in neurons under the control of Scer\GAL4elav-C155, or in both neurons or glia.
Dmtne01970 is rescued by Scer\GAL4elav-C155/DmtnUAS.cHa
Dmtne01970 is rescued by Scer\GAL4elav-C155/DmtnUAS.cHa/Scer\GAL4repo
Dmtne01970 is partially rescued by DmtnUAS.cHa/Scer\GAL4repo
Expression of DmtnScer\UAS.cHa under the control of either Scer\GAL4elav-C155 (neurons), Scer\GAL4repo (glia) or both, rescues the lethality associated with Dmtne01970. The optic lobes of all Dmtne01970 flies rescued by expression of DmtnScer\UAS.cHa in either just neurons or both neurons and glia are normal in appearance. The optic lobes of flies rescued in the glia only are less developed, as shown by a wider angle between the lamina and medulla neuropils, due to partial rotation of the medulla neuropil and by aberrant targeting of retinal axons.