Larvae expressing RhebUAS.cPa under the control of Scer\GAL4ci.PC exhibit a small imaginal disc anterior compartment.
Expression of RhebUAS.cPa under the control of Scer\GAL4Su(H).GBE (in combination with tub-Gal80[ts] to restrict expression to the adult stage) leads to an increase in the cell size of enteroblasts in adult guts when compared to controls.
Third instar larvae expressing RhebUAS.cPa under the control of Scer\GAL4AB1 do not show significant changes in the size of salivary gland cells, as compared to controls.
Expression of RhebScer\UAS.cPa under the control of Scer\GAL4insc-Mz1407 is capable of driving central brain neuroblast reactivation in the absence of dietary amino acids.
The expression of RhebScer\UAS.cPa under the control of Scer\GAL4en-e16E leads to a significant increase in the wing posterior compartment area, as compared to controls.
Expression of RhebScer\UAS.cPa under the control of Scer\GAL4phm.PO leads to decreased number of autophagic vesicles (marked with Atg8a protein).
The expression of RhebScer\UAS.cPa under the control of Scer\GAL4E(spl)m6-BFM.PF leads to significantly increased numbers of abdominal lateral and dorsal, but not ventral, adult muscle precursor cells in third instar larvae, as compared to controls; this expression does not affect the number of mitotic adult muscle precursor cells at embryonic stages, as compared to controls.
Expression via Scer\GAL4wor.PA and Scer\GAL80ase.PN does not prevent the normal shrinkage and disappearance of pupal neuroblasts.
Expression of RhebScer\UAS.cPa under the control of Scer\GAL4da.G32 results in an increase in larval body weight compared to controls.
Flies expressing RhebScer\UAS.cPa in the midgut, under the control of Scer\GAL4esg-NP5130 and Scer\GAL80ts.αTub84B at the restrictive temperature of 29[o]C for two weeks, results in considerably fewer epithelial midgut cells, accounting for 10.4% of the total population. Some of the remaining intestinal stem cells are larger.
Overexpression of RhebScer\UAS.cPa under the control of Scer\GAL4GMR.PF increases S6k phosphorylation.
Expression of RhebScer\UAS.cPa under the control of Scer\GAL4Mef2.PR is able to completely suppress the formation of autophagosomes in the muscles of chloroquine-treated larvae starved on low-nutrient food for 6 hours.
Scer\GAL4elav.PLu-mediated expression of RhebScer\UAS.cPa produces phototaxis deficits and a significantly lower phototaxis index. It also results in a failure of some R7 and R8 photoreceptors to terminate at their proper locations, produces substantial synaptic overgrowth at the larval neuromuscular junction, and increased excitatory junctional potentials.
The Scer\GAL4elav.PLu, RhebScer\UAS.cPa phototaxis deficits are significantly rescued when flies are reared on a yeast-restricted or calorie-restricted diet.
Raised at 25[o]C, the Scer\GAL4elav.PLu, RhebScer\UAS.cPa axon guidance phenotype is significantly rescued when flies are reared on a yeast-restricted or calorie-restricted or sugar-restricted diet.
Raised at 21[o]C, the Scer\GAL4elav-C155, RhebScer\UAS.cPa flies show a mild axon guidance phenotype that is significantly rescued when flies are reared on a yeast-restricted or calorie-restricted diet.
The Scer\GAL4elav.PLu, RhebScer\UAS.cPa synaptic overgrowth and increased excitatory junctional potential phenotypes cannot be rescued by dietary restriction. Flies raised on a sugar restricted diet actually show an increase in synaptic overgrowth.
Expression of RhebScer\UAS.cPa in mushroom body γ-neurons, under the control of Scer\GAL4Tab2-201Y does not affect mushroom body morphology.
Overexpression of RhebScer\UAS.cPa using either Scer\GAL4elav-C155 or Scer\GAL4P2.4.Pdf increases ethanol sensitivity.
Expression of RhebScer\UAS.cPa under the control of Scer\GAL4sca.PU in the adult thorax leads to an increase in the frequency of bristle twinning, and delay or premature arrest of the cell cycle, as compared to controls.
Overexpression of RhebScer\UAS.cPa via Scer\GAL4GMR.PF causes a hyperplastic phenotype in the eye.
Expression of RhebScer\UAS.cPa in the developing eye under the control of Scer\GAL4GMR.PF results in a rough eye phenotype with bristle disorganization.
Expression of RhebScer\UAS.cPa driven by Scer\GAL4ap-md544 in the dorsal epithelial of the wing disc results in enlargement of the dorsal compartment, which causes the wing to curve downwards. When expression of RhebScer\UAS.cPa is driven by Scer\GAL4ap-md544 in the posterior compartment of the wing, the posterior area is increased but cell density is lower and total cell number is not significantly different to wild type. Therefore, cell size is increased. The anterior compartment of these wings is reduced compared to wild type, while the cell density is increased.
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neurophysiology phenotype, enhanceable by AMPKαTD.UAS, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4Su(H).GBE has increased cell size | adult stage phenotype, suppressible by zfh2GD4506, Scer\GAL4Su(H).GBE
RhebUAS.cPa, Scer\GAL4Su(H).GBE has increased cell size | adult stage phenotype, suppressible by zfh2HMC03043, Scer\GAL4Su(H).GBE
RhebUAS.cPa, Scer\GAL4en-e16E has abnormal size | adult stage phenotype, suppressible by nclbNIG.6751R, Scer\GAL4en-e16E
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neuroanatomy phenotype, suppressible by mTorΔ6B/Tor[+]
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal phototaxis phenotype, suppressible by mTorΔ6B/Tor[+]
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neuroanatomy phenotype, suppressible by AMPKαTD.UAS, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal phototaxis phenotype, suppressible by AMPKαTD.UAS, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neuroanatomy phenotype, suppressible by raptorGD5138, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neuroanatomy phenotype, suppressible by S6kGD6646, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4GMR.PF has visible phenotype, suppressible by Sesnd04539, Scer\GAL4GMR.PF
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neuroanatomy phenotype, non-suppressible by rictorΔ2/rictorΔ1
RhebUAS.cPa, Scer\GAL4elav.PLu has abnormal neuroanatomy phenotype, non-suppressible by Sin1e03756/Sin1e03756
Scer\GAL4ci.PC/RhebUAS.cPa is an enhancer of increased cell death | larval stage | somatic clone phenotype of RpS23R67K
RhebUAS.cPa/Scer\GAL4ppk.PG is an enhancer of abnormal neuroanatomy | pupal stage | somatic clone phenotype of Mical15256
RhebUAS.cPa, Scer\GAL4elav-C155 is an enhancer of abnormal neuroanatomy phenotype of Hsap\HTT98Q.Ex1.UAS.EGFP.Tag:NLS(Unk), Scer\GAL4elav-C155
RhebUAS.cPa/Scer\GAL4pHCl-2.PR is a suppressor of abnormal developmental rate phenotype of pHCl-2pTV-Cherry
RhebUAS.cPa/Scer\GAL4pHCl-2.PR is a suppressor of decreased rate of feeding behavior | larval stage phenotype of pHCl-2pTV-Cherry
RhebUAS.cPa/Scer\GAL4Tab2-201Y is a suppressor | partially of abnormal neuroanatomy | somatic clone phenotype of Hr51LL04325
RhebUAS.cPa, Scer\GAL4NP0001 is a non-suppressor of increased cell size phenotype of Atg9HMS01246, Scer\GAL4NP0001
RhebUAS.cPa/Scer\GAL4ppk.PG is a non-suppressor of abnormal neuroanatomy | larval stage phenotype of pathdg50/Df(3L)BSC773
RhebUAS.cPa, Scer\GAL4elav-C155 is a non-suppressor of abnormal neuroanatomy phenotype of Scer\GAL4elav-C155, Vap33P58S.cRa.UAS
PIP4K29, RhebUAS.cPa, Scer\GAL4AB1 has increased cell size | third instar larval stage phenotype
RhebUAS.cPa, Scer\GAL4ppk.PG, pathA.UAS.GFP has abnormal neuroanatomy phenotype
RhebUAS.cPa, Scer\GAL4elav.PLu has embryonic/larval neuromuscular junction phenotype, enhanceable by AMPKαTD.UAS, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4sca.PU has mesothoracic bristle | adult stage | increased number phenotype, non-enhanceable by Rab11UASp.YFP, Scer\GAL4sca.PU
RhebUAS.cPa, Scer\GAL4sca.PU has mesothoracic bristle | adult stage | increased number phenotype, non-enhanceable by nufEP3324, Scer\GAL4sca.PU
RhebUAS.cPa, Scer\GAL4insc-Mz1407 has neuroblast | third instar larval stage | nutrition conditional phenotype, suppressible by ChroKK105370, Scer\GAL4insc-Mz1407
RhebUAS.cPa, Scer\GAL4en-e16E has wing posterior compartment phenotype, suppressible by nclbNIG.6751R, Scer\GAL4en-e16E
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R7 phenotype, suppressible by mTorΔ6B/Tor[+]
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R8 phenotype, suppressible by mTorΔ6B/Tor[+]
RhebUAS.cPa, Scer\GAL4elav.PLu has embryonic/larval neuromuscular junction phenotype, suppressible by mTorΔ6B/Tor[+]
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R7 phenotype, suppressible by AMPKαTD.UAS, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R8 phenotype, suppressible by AMPKαTD.UAS, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R7 phenotype, suppressible by raptorGD5138, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R8 phenotype, suppressible by raptorGD5138, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R7 phenotype, suppressible by S6kGD6646, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R8 phenotype, suppressible by S6kGD6646, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has embryonic/larval neuromuscular junction phenotype, suppressible by rictorΔ2/rictorΔ1
RhebUAS.cPa, Scer\GAL4elav.PLu has embryonic/larval neuromuscular junction phenotype, suppressible by Sin1e03756/Sin1e03756
RhebUAS.cPa, Scer\GAL4GMR.PF has eye phenotype, suppressible by Sesnd04539, Scer\GAL4GMR.PF
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R7 phenotype, non-suppressible by rictorΔ2/rictorΔ1
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R8 phenotype, non-suppressible by rictorΔ2/rictorΔ1
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R7 phenotype, non-suppressible by Sin1e03756/Sin1e03756
RhebUAS.cPa, Scer\GAL4elav.PLu has photoreceptor cell R8 phenotype, non-suppressible by Sin1e03756/Sin1e03756
RhebUAS.cPa, Scer\GAL4elav.PLu has embryonic/larval neuromuscular junction phenotype, non-suppressible by raptorGD5138, Scer\GAL4elav.PLu
RhebUAS.cPa, Scer\GAL4elav.PLu has embryonic/larval neuromuscular junction phenotype, non-suppressible by S6kGD6646, Scer\GAL4elav.PLu
Scer\GAL4ci.PC/RhebUAS.cPa is an enhancer of imaginal disc phenotype of RpS23R67K
RhebUAS.cPa/Scer\GAL4ppk.PG is an enhancer of larval dorsal multidendritic neuron ddaC | pupal stage | somatic clone phenotype of Mical15256
RhebUAS.cPa, Scer\GAL4sca.PU is an enhancer of mesothoracic bristle | adult stage | increased number phenotype of Scer\GAL4sca.PU, l(2)gl3A.UAS
Scer\GAL4GMR.PF, RhebUAS.cPa is an enhancer of eye phenotype of Hsap\HTT152Q.Ex1.UAS.EGFP, Hsap\HTT48Q.Ex1.UAS.EGFP.Tag:NLS(Unk), Scer\GAL4GMR.PF
Scer\GAL4GMR.PF, RhebUAS.cPa is an enhancer of pigment cell phenotype of Hsap\HTT152Q.Ex1.UAS.EGFP, Hsap\HTT48Q.Ex1.UAS.EGFP.Tag:NLS(Unk), Scer\GAL4GMR.PF
Scer\GAL4ninaE.PU/RhebUAS.cPa is a suppressor of vesicle | pupal stage | conditional phenotype of PIP4K29
Scer\GAL4ninaE.PU/RhebUAS.cPa is a suppressor of multivesicular body | pupal stage | conditional phenotype of PIP4K29
RhebUAS.cPa/Scer\GAL4Tab2-201Y is a suppressor | partially of gamma Kenyon cell | somatic clone phenotype of Hr51LL04325
RhebUAS.cPa/Scer\GAL4btl.PS is a non-suppressor of terminal tracheal cell | somatic clone | larval stage phenotype of Archeasedsj-169
Scer\GAL4ninaE.PU/RhebUAS.cPa is a non-suppressor of photoreceptor neuron | pupal stage | conditional phenotype of PIP4K29
RhebUAS.cPa, Scer\GAL4NP0001 is a non-suppressor of adult midgut epithelium phenotype of Atg9HMS01246, Scer\GAL4NP0001
RhebUAS.cPa/Scer\GAL4bs.PM is a non-suppressor of terminal tracheal cell | somatic clone | third instar larval stage phenotype of Vha13cnj-356
RhebUAS.cPa/Scer\GAL4ppk.PG is a non-suppressor of larval multidendritic class IV neuron phenotype of pathdg50/Df(3L)BSC773
RhebUAS.cPa, Scer\GAL4elav-C155 is a non-suppressor of terminal bouton phenotype of Scer\GAL4elav-C155, Vap33P58S.cRa.UAS
PIP4K29, RhebUAS.cPa, Scer\GAL4AB1 has fat cell | third instar larval stage phenotype
RhebUAS.cPa, Scer\GAL4ppk.PG, pathA.UAS.GFP has larval multidendritic class IV neuron phenotype
Hr51LL04325, RhebUAS.cPa, Scer\GAL4Tab2-201Y has alpha/beta Kenyon cell | somatic clone phenotype
PIP4K29 third instar larvae expressing RhebUAS.cPa under the control of Scer\GAL4AB1 show significantly bigger salivary gland cells, as compared to PIP4K29 single mutants.
The expression of RhebScer\UAS.cPa under the control of Scer\GAL4ninaE.PU does not suppress the expansion in endosome-like vesicles and multivesicular bodies observed in the photoreceptors of PIP4K29 homozygous late pupae reared in light conditions.
The ability of Scer\GAL4insc-Mz1407-driven expression of RhebScer\UAS.cPa to induce central brain neuroblast reactivation in the absence of dietary amino acids is prevented by co-expression of ChroKK105370.
The increased wing posterior compartment area induced by the expression of RhebScer\UAS.cPa under the control of Scer\GAL4en-e16E is suppressed by the co-expression of nclbNIG.6751R.
The co-expression of RhebScer\UAS.cPa does not suppress the increased midgut cell size resulting from the expression of Atg9HMS01246 under the control of Scer\GAL4Myo31DF-NP0001.
Scer\GAL4ppk.PG-mediated co-expression of pathA.Scer\UAS.T:Avic\GFP and RhebScer\UAS.cPa promote dendritic growth, whereas expression of either alone has no such effect.
Expression of RhebScer\UAS.cPa does not suppress the enlarged bouton phenotype seen when Vap-33AP58S.cRa.Scer\UAS is expressed under the control of Scer\GAL4elav-C155.
Expression of RhebScer\UAS.cPa under the control of Scer\GAL4ppk.PG enhances the dendrite pruning defects seen in Mical15256 mutant ddaC neuron clones at 16 hours after puparium formation.
Heterozygosity for TorΔ6B in a RhebScer\UAS.cPa, Scer\GAL4elav.PLu background rescues the phototaxis phenotype and photoreceptor axon guidance abnormalities to almost control levels, and causes a significant rescue of the synapse overgrowth phenotype.
Co-expression of SNF1ATD.Scer\UAS significantly rescues the phototaxis and axon guidance phenotypes, while it enhances the synapse overgrowth and excitatory junctional potential phenotypes, of RhebScer\UAS.cPa, Scer\GAL4elav.PLu flies.
Co-expression of raptorGD5138 or S6kGD6646 significantly rescues the axon guidance phenotypes of RhebScer\UAS.cPa, Scer\GAL4elav.PLu flies.
The axon guidance phenotypes of RhebScer\UAS.cPa, Scer\GAL4elav.PLu flies are not significantly rescued in a rictorΔ1/rictorΔ2 or Sin1e03756/Sin1e03756 background.
Co-expression of raptorGD5138 or S6kGD6646 does not rescue the RhebScer\UAS.cPa, Scer\GAL4elav.PLu synapse overgrowth phenotype.
The RhebScer\UAS.cPa, Scer\GAL4elav.PLu synapse overgrowth phenotype is significantly rescued in a rictorΔ1/rictorΔ2 or Sin1e03756/Sin1e03756 background.
Expression of RhebScer\UAS.cPa in Hr51LL04325 MARCM neuroblast clones partially suppresses the developmental regrowth defect. In addition these double mutants exhibit severe axon guidance defects. In these clones, γ axons do not occupy the entire adult lobe but instead grow to the dorsal and ventral extremities of the adult γ-lobe and in some cases only to its ventral portion.
Co-expression of Rab11Scer\UAS.P\T.T:Avic\GFP-YFP or nufEP3324 does not enhance the bristle twinning phenotype of flies expressing RhebScer\UAS.cPa under the control of Scer\GAL4sca.PU.
Co-expression of RhebScer\UAS.cPa enhances the bristle twinning phenotype seen in flies expressing l(2)gl3A.Scer\UAS under the control of Scer\GAL4sca.PU.
Co-expression of Sesnd04539 with RhebScer\UAS.cPa via Scer\GAL4GMR.PF suppresses the RhebScer\UAS.cPa hyperplastic eye phenotype.
Overexpression of RhebScer\UAS.cPa in the developing eye enhances the phenotype seen in mutant flies co-expressing Hsap\HTT152Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP and Hsap\HTT48Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 under the control of Scer\GAL4GMR.PF, with a severe rough eye phenotype and enhancement of pigment cell loss.
Overexpression of RhebScer\UAS.cPa in the developing eye of Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 mutants (both transgene under the control of Scer\GAL4GMR.PF results in a rough eye phenotype with bristle disorganization.
Co-expression of RhebScer\UAS.cPa in a Hsap\HTT98Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 mutant brain (with both transgenes under the control of Scer\GAL4elav-C155) does not significantly increase the average number of brain aggregate inclusions compared to flies expressing Hsap\HTT98Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 alone, but does increase the average aggregate size.