UAS regulatory sequences drive expression of a mutated form of Hsap\LRRK2 which contains the familial Parkinson's disease-associated G2019S mutation.
Flies expressing Hsap\LRRK2G2019S.Scer\UAS.cMa under the control of either Scer\GAL4ple.PF or Scer\GAL4Ddc.PL show a reduced lifespan compared to controls. 5 day old flies expressing Hsap\LRRK2G2019S.Scer\UAS.cMa under the control of Scer\GAL4ple.PF exhibit loss of dorsomedial posterior protocerebral (PPM1) and dorsolateral posterior protocerebral (PPL1) dopaminergic neurons, ascompared to controls.
Hsap\LRRK2G2019S.UAS.cMa, Scer\GAL4ple.PF has short lived phenotype, suppressible | partially by Rab32UASp.YFP, Scer\GAL4ple.PF
Hsap\LRRK2G2019S.UAS.cMa, Scer\GAL4ple.PF has short lived phenotype, suppressible | partially by Rab32Q79L.UASp.YFP, Scer\GAL4ple.PF
Hsap\LRRK2G2019S.UAS.cMa, Scer\GAL4ple.PF has abnormal neuroanatomy | adult stage phenotype, suppressible by Rab32Q79L.UASp.YFP, Scer\GAL4ple.PF
Hsap\LRRK2G2019S.UAS.cMa, Scer\GAL4ple.PF has short lived phenotype, non-suppressible by Rab32T33N.UASp.YFP, Scer\GAL4ple.PF
Hsap\LRRK2G2019S.UAS.cMa, Scer\GAL4ple.PF has dopaminergic PPM1 neuron phenotype, suppressible by Rab32Q79L.UASp.YFP, Scer\GAL4ple.PF
Hsap\LRRK2G2019S.UAS.cMa, Scer\GAL4ple.PF has dopaminergic PPL1 neuron phenotype, suppressible by Rab32Q79L.UASp.YFP, Scer\GAL4ple.PF
Co-expression of ltdQ79L.Scer\UAS.P\T.T:Avic\GFP-YFP rescues the reduced lifespan and loss of dorsomedial posterior protocerebral and dorsolateral posterior protocerebral dopaminergic neurons seen in flies expressing Hsap\LRRK2G2019S.Scer\UAS.cMa under the control of Scer\GAL4ple.PF.