UAS regulatory sequences drive expression of full length Hsap\DTNBP1 cDNA.
Scer\GAL4elav-C155/Hsap\DTNBP1UAS.cSa is a suppressor of abnormal neurophysiology | larval stage phenotype of Dysbe01028
Scer\GAL4elav-C155/Hsap\DTNBP1UAS.cSa is a suppressor of abnormal memory | adult stage phenotype of Dysbe01028
Scer\GAL4repo/Hsap\DTNBP1UAS.cSa is a suppressor of abnormal locomotor behavior | adult stage phenotype of Dysbe01028
Scer\GAL4elav-C155/Hsap\DTNBP1UAS.cSa is a suppressor of embryonic/larval neuromuscular junction | larval stage phenotype of Dysbe01028
Pan-neuronal expression of Hsap\DTNBP1Scer\UAS.cSa under the control of Scer\GAL4elav-C155 rescues the larval neuromuscular junction excitatory junctional current defects and the adult short term memory defects observed in dysbe01028 mutants.
Expression of Hsap\DTNBP1Scer\UAS.cSa in the glia under the control of Scer\GAL4repo partially suppresses the locomotor defects seen in dysbe01028 mutants. The increase in dopamine levels seen in dysbe01028 mutant heads is also suppressed.