Amino acid replacement: Y1383C.
The Y1383C mutation was reported relative to Lrrk-PB. analogous mutation in human LRRK2 implicated in Parkinson;disease 8; mutation carried on in vitro construct; site of nucleotide substitution in fly gene and specific disease association inferred by FlyBase curator.
Axonal transport of mitochondria is disrupted in larval motor neurons expressing LrrkY1383C.Scer\UAS under the control of Scer\GAL4D42.
Flies expressing LrrkY1383C.Scer\UAS under the control of Scer\GAL4D42 show locomotor defects.
Flies expressing LrrkY1383C.Scer\UAS under the control of Scer\GAL4ple.PG do not show a progressive reduction in electroretinogram amplitude (there is no significant difference in the amplitude seen in 3 and 28 day old flies).
60 day old adults expressing LrrkY1383C.Scer\UAS under the control of Scer\GAL4ple.PF show a significant reduction in the number of dopaminergic neurons in the protocerebral posterior medial 1 and 2 clusters and in the protocerebral posterior lateral 1 cluster compared to control flies, although the number of neurons in the protocerebral posterior medial 3 cluster is unaffected in the mutant flies.
Flies expressing LrrkY1383C.Scer\UAS under the control of Scer\GAL4da.G32 show significantly higher sensitivity to paraquat and to hydrogen peroxide compared to control flies.
LrrkY1383C.UAS, Scer\GAL4ple.PF has abnormal neuroanatomy | adult stage phenotype, suppressible by ThorUAS.cMa, Scer\GAL4ple.PF
Scer\GAL4nSyb.PP/LrrkY1383C.UAS is an enhancer of abnormal locomotor behavior | adult stage phenotype of Hsap\SNCAQUAS.cOa, Ncra\QFQF2.nSyb
Scer\GAL4nSyb.PP/LrrkY1383C.UAS is an enhancer of decreased cell number | adult stage phenotype of Hsap\SNCAQUAS.cOa, Ncra\QFQF2.nSyb
LrrkY1383C.UAS, Scer\GAL4GMR.PF is an enhancer of visible phenotype of Scer\GAL4GMR.PF, foxoUAS.cKb
LrrkY1383C.UAS, Scer\GAL4elav.Switch.PO, foxoUAS.cKb has short lived | RU486 conditional phenotype
LrrkY1383C.UAS, Scer\GAL4elav.Switch.PO, foxoUAS.cKb has abnormal neuroanatomy | adult stage | RU486 conditional phenotype
LrrkY1383C.UAS, Scer\GAL4ple.PF has dopaminergic neuron phenotype, suppressible by ThorUAS.cMa, Scer\GAL4ple.PF
Scer\GAL4nSyb.PP/LrrkY1383C.UAS is an enhancer of outer medulla | adult stage phenotype of Hsap\SNCAQUAS.cOa, Ncra\QFQF2.nSyb
Scer\GAL4nSyb.PP/LrrkY1383C.UAS is an enhancer of medulla intrinsic columnar neuron | adult stage | decreased number phenotype of Hsap\SNCAQUAS.cOa, Ncra\QFQF2.nSyb
Scer\GAL4nSyb.PP/LrrkY1383C.UAS is an enhancer of dopaminergic medulla neuron | adult stage | decreased number phenotype of Hsap\SNCAQUAS.cOa, Ncra\QFQF2.nSyb
LrrkY1383C.UAS, Scer\GAL4GMR.PF is an enhancer of eye phenotype of Scer\GAL4GMR.PF, foxoUAS.cKb
LrrkY1383C.UAS, Scer\GAL4elav.Switch.PO, foxoUAS.cKb has dopaminergic neuron | RU486 conditional phenotype
LrrkY1383C.UAS, Scer\GAL4elav.Switch.PO, foxoUAS.cKb has dopaminergic PPL1 neuron | RU486 conditional phenotype
LrrkY1383C.UAS, Scer\GAL4elav.Switch.PO, foxoUAS.cKb has dopaminergic PPM3 neuron | RU486 conditional phenotype
The severity of the eye defects caused by expression of foxoScer\UAS.cKb under the control of Scer\GAL4GMR.PF are enhanced by co-expression of LrrkY1383C.Scer\UAS.
Co-expression of foxoScer\UAS.cKb and LrrkY1383C.Scer\UAS under the control of Scer\GAL4elav.Switch.PO in the presence of RU486 throughout the lifespan results in a reduction in lifespan. These flies show an age-dependent decrease in the number of PPM1/2, PPM3 and PPL1 neurons.
The decrease in the number of dopaminergic neurons in the protocerebral posterior medial 1 and 2 clusters and in the protocerebral posterior lateral 1 cluster that is seen in 60 day old adults expressing LrrkY1383C.Scer\UAS under the control of Scer\GAL4ple.PF is suppressed by co-expression of ThorScer\UAS.cMa.