The P{GawB} insertion in P{GawB}Hr39c739 has been replaced with a P{Mae-UAS.6.11} element, generating the P{Mae-UAS.6.11}Hr39C13 insertion 9.5kb upstream of the Hr39 ATG codon. The Scer\UAS regulatory sequences present in the P{Mae-UAS.6.11} element can be used to drive overexpression of the endogenous Hr39 gene.
Hr39C13 adults show a mushroom body axon pruning phenotype as revealed by the presence of some adult unpruned vertical gamma axons; the unpruned axon phenotype is also apparent during metamorphosis.
Ectopic expression of Hr39C13 driven by Scer\GAL4Tab2-201Y in developing γ neurons blocks pruning. Although some γ neurons seem pruned normally, 100% of the mushroom bodies predominantly display γ neurons that retain their larval characteristics. In mutant neuroblast clones, there is a mixture of unpruned and apparently pruned &gr; neurons. Similarly, in two-cell mutant clones, two mutant neurons are clearly unpruned whereas two others appear normal. Only γ neurons appear affected by Hr39C13 ectopic expression in adult mushroom body neurons.
Hr39C13, Scer\GAL4Tab2-201Y has abnormal neuroanatomy phenotype, enhanceable by EcRB1.UAS, Scer\GAL4Tab2-201Y
Hr39C13, Scer\GAL4Tab2-201Y has gamma Kenyon cell phenotype, enhanceable by EcRB1.UAS, Scer\GAL4Tab2-201Y
Expression of EcRB1.Scer\UAS in Hr39C13 neuroblast clones (under the control of Scer\GAL4Tab2-201Y) restores wild-type γ neuron remodelling.