UASt regulatory sequences drive expression of an inverted repeat.
Expression of PEKGD5584 under the control of Scer\GAL4109(2)80 does not significantly affect the total branch length of the dendritic arbor in class IV ddaC neurons in third instar larvae.
Expression of PEKGD5584 under the control of Scer\GAL4bun-GSG5961, using RU486 food supplementation to induce the expression, extends adult lifespan relative to controls.
Adults expressing PEKGD5584 under the control of Scer\GAL4elav.PLu (in the presence of Dcr-2Scer\UAS.cDa to increase the efficiency of RNAi) do not show a significant defect in avoidance of noxious temperature (46[o]C) compared to control flies.
Scer\GAL4Act.PU/PEKGD5584 is a non-enhancer of decreased cell number | larval stage | somatic clone phenotype of scrib1
PEKGD5584, Scer\GAL4nub.PU is a suppressor of increased cell death | larval stage phenotype of Gp93NIG.5520R, Scer\GAL4nub.PU
PEKGD5584, Scer\GAL4109(2)80 is a suppressor | partially of abnormal neuroanatomy | third instar larval stage phenotype of Scer\GAL4109(2)80, prelUAS.Tag:HA
Scer\GAL4elav.PU/PEKGD5584 is a suppressor of abnormal neuroanatomy | adult stage phenotype of park25
Scer\GAL4elav.PU/PEKGD5584 is a suppressor | partially of abnormal neuroanatomy | adult stage phenotype of Pink1B9
PEKGD5584, Scer\GAL4NP5130 is a suppressor of increased occurrence of cell division phenotype of Scer\GAL4NP5130, hepUAS.cBa
PEKGD5584, Scer\GAL4NP5130 is a suppressor of increased occurrence of cell division phenotype of NRNAi.P.UAS, Scer\GAL4NP5130
PEKGD5584, Scer\GAL4NP5130 is a suppressor of increased occurrence of cell division | adult stage phenotype of Ero1LGD3577, Scer\GAL4NP5130
PEKGD5584, Scer\GAL4da.G32 is a suppressor | partially of abnormal developmental rate | larval stage phenotype of PPP1R15GD5953, Scer\GAL4da.G32
Scer\GAL4Act.PU/PEKGD5584 is a non-suppressor of decreased cell number | somatic clone | larval stage phenotype of scrib1
PEKGD5584, PPP1R15GD5953, Scer\GAL4da.G32 has partially lethal phenotype
Scer\GAL4Act.PU/PEKGD5584 is a non-enhancer of eye-antennal disc | somatic clone phenotype of scrib1
PEKGD5584, Scer\GAL4nub.PU is a suppressor of wing disc | larval stage phenotype of Gp93NIG.5520R, Scer\GAL4nub.PU
PEKGD5584, Scer\GAL4109(2)80 is a suppressor | partially of abdominal dorsal multidendritic neuron ddaC | third instar larval stage phenotype of Scer\GAL4109(2)80, prelUAS.Tag:HA
PEKGD5584, Scer\GAL4109(2)80 is a suppressor | partially of dendrite | third instar larval stage phenotype of Scer\GAL4109(2)80, prelUAS.Tag:HA
Scer\GAL4elav.PU/PEKGD5584 is a suppressor of dopaminergic PPL1 neuron | adult stage phenotype of park25
Scer\GAL4elav.PU/PEKGD5584 is a suppressor | partially of dopaminergic PPL1 neuron | adult stage phenotype of Pink1B9
PEKGD5584, Scer\GAL4NP5130 is a suppressor of adult gut phenotype of Scer\GAL4NP5130, hepUAS.cBa
PEKGD5584, Scer\GAL4NP5130 is a suppressor of adult gut phenotype of NRNAi.P.UAS, Scer\GAL4NP5130
PEKGD5584, Scer\GAL4NP5130 is a suppressor of intestinal stem cell | adult stage phenotype of Ero1LGD3577, Scer\GAL4NP5130
Scer\GAL4Act.PU/PEKGD5584 is a non-suppressor of eye-antennal disc | somatic clone phenotype of scrib1
The shortening of the dendritic arbor in class IV ddaC neurons in third instar larvae expressing prelScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4109(2)80 is strongly mitigated by co-expression of any of PEKGD5584.
Expression of PEKGD5584 under the control of Scer\GAL4elav.PU significantly rescues the loss of dopaminergic neurons characteristic for either Pink1B9 or park25/park25 mutant adults.
The increased cell proliferation in the adult gut expressing hepScer\UAS.cBa or Ero1LGD3577 or NdsRNA.P.Scer\UAS under the control of Scer\GAL4esg-NP5130 (using tub-gal80[ts] to limit the time of expression) is suppressed by co-expression of PEKGD5584.
Co-expression of PEKGD5584 modestly rescues the developmental delay phenotype of animals expressing Gadd34GD5953 under the control of Scer\GAL4da.G32. However, these animals often die during eclosion from the pupal case, and surviving adults show severe mobility defects and have strongly reduced longevity.