UASt regulatory sequences drive expression of RhoGAPp190 tagged with Tag:MYC.
Expression of RhoGAPp190Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4ptc-559.1 results in occasional cells with multiple hairs in the wing.
Expression of RhoGAPp190Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4OK107 results in axon growth defects in the mushroom body.
Expression of RhoGAPp190Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4OK107 results in overextension of the dorsal lobe axons in the mushroom body.
Scer\GAL4ptc-559.1/RhoGAPp190UAS.Tag:MYC is an enhancer of visible phenotype of mwh6/mwh1
RhoGAPp190UAS.Tag:MYC, Scer\GAL4en-e16E is a suppressor of visible phenotype of LIMK1UAS.cCa, Scer\GAL4en-e16E
RhoGAPp190UAS.Tag:MYC, Scer\GAL4ey-OK107 is a suppressor of abnormal neuroanatomy phenotype of LIMK1UAS.Tag:HA, Scer\GAL4ey-OK107
Scer\GAL4ptc-559.1/RhoGAPp190UAS.Tag:MYC is an enhancer of wing hair | increased number phenotype of mwh6/mwh1
RhoGAPp190UAS.Tag:MYC, Scer\GAL4en-e16E is a suppressor of wing phenotype of LIMK1UAS.cCa, Scer\GAL4en-e16E
RhoGAPp190UAS.Tag:MYC, Scer\GAL4ey-OK107 is a suppressor of adult mushroom body phenotype of LIMK1UAS.Tag:HA, Scer\GAL4ey-OK107
LIMK1UAS.cCa, RhoGAPp190UAS.Tag:MYC, Scer\GAL4en-e16E has crossvein | ectopic phenotype
Expression of RhoGAPp190Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4ptc-559.1 enhances the mwh1/mwh6 multiple wing hair phenotype.
Co-expression of RhoGAPp190Scer\UAS.T:Hsap\MYC suppresses the mutant wing phenotype caused by expression of LIMK1Scer\UAS.cCa under the control of Scer\GAL4en-e16E (the % of wings with normal morphology at 18oC is increased from 9% to 85%). Approximately 63% of the flies show a mild extra crossvein phenotype.
Scer\GAL4elav.PLu/RhoGAPp190UAS.Tag:MYC partially rescues RhoGAPp1902
Co-expression of RhoGAPp190Scer\UAS.T:Hsap\MYC rescues the premature defasciculation phenotype seen in the ISNb axons in embryos expressing RhoGAPp190dsRNA.GAP.Scer\UAS under the control of Scer\GAL4elav.PLu.
Expression of RhoGAPp190Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4elav.PLu partially rescues the ISNb axon guidance defects seen in embryos both maternally and zygotically mutant for RhoGAPp1902.