Mutations in babo block γ-neuron remodelling.
The brain lobes of mutant third instar larvae are 25-40% smaller than those of heterozygous controls.
babounspecified has abnormal neuroanatomy phenotype, non-enhanceable by Hr39c739
Hr39c739, babounspecified has abnormal neuroanatomy phenotype, non-enhanceable by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
babounspecified has abnormal neuroanatomy phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
Hr39c739, babounspecified has abnormal neuroanatomy phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
babounspecified has abnormal neuroanatomy phenotype, non-suppressible by Hr39c739
Hr39c739, babounspecified has abnormal neuroanatomy phenotype, non-suppressible by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
babounspecified has gamma Kenyon cell phenotype, non-enhanceable by Hr39c739
Hr39c739, babounspecified has gamma Kenyon cell phenotype, non-enhanceable by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
babounspecified has gamma Kenyon cell phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
Hr39c739, babounspecified has gamma Kenyon cell phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
babounspecified has gamma Kenyon cell phenotype, non-suppressible by Hr39c739
Hr39c739, babounspecified has gamma Kenyon cell phenotype, non-suppressible by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
Restoration of EcR, through expression of EcRB1.Scer\UAS in a babounspecified mutant background partially rescues the γ-neuron remodelling defects in these mutants.
A Hr39c739 homozygous mutant background does not affect the mutant pruning phenotype seen in babounspecified mutant γ neurons.
Expression of ftz-f1β.Scer\UAS.cBa in a babounspecified Hr39c739 double mutant background, under the control of Scer\GAL4Tab2-201Y does not affect the mutant pruning phenotype seen in these double mutant γ neurons.
Restoration of EcR, through expression of EcRB1.Scer\UAS in a babounspecified Hr39c739 double mutant background, under the control of Scer\GAL4Tab2-201Y partially rescues the γ-neuron remodelling defects in these mutants.