Expression of Rac1Y40C.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4OK107 does not disrupt mushroom body axon patterning in a wild-type background.
Rac1Y40C.UAS.Tag:MYC, NavA384, NavΔ, Scer\GAL4ey-OK107 is a non-suppressor of abnormal neuroanatomy phenotype of LIMK1UAS.Tag:HA, Scer\GAL4ey-OK107
Rac1Y40C.UAS.Tag:MYC, NavA384, NavΔ, Scer\GAL4ey-OK107 is a non-suppressor of mushroom body phenotype of LIMK1UAS.Tag:HA, Scer\GAL4ey-OK107
Rac1Y40C.UAS.Tag:MYC, NavA384, NavΔ, Scer\GAL4ey-OK107 is a non-suppressor of adult mushroom body alpha-lobe phenotype of LIMK1UAS.Tag:HA, Scer\GAL4ey-OK107
Rac1Y40C.UAS.Tag:MYC, NavA384, NavΔ, Scer\GAL4ey-OK107 is a non-suppressor of adult mushroom body beta-lobe phenotype of LIMK1UAS.Tag:HA, Scer\GAL4ey-OK107
Expression of Rac1Y40C.Scer\UAS.T:Hsap\MYC suppresses the axon growth defect and F-actin elevation seen in the α/β mushroom body lobes when LIMK1Scer\UAS.T:Ivir\HA1 is expressed under the control of Scer\GAL4ey-OK107. This suppression does not occur in a sickΔ/sickA384 mutant background.
Mushroom body axon growth defects in single-cell Rac1J11 Rac2Δ MtlΔ γ neuron clones are largely rescued by expression of Rac1Y40C.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4OK107. 81% of axons in Rac1J11 Rac2Δ mushroom body clones show mutant phenotypes, predominantly guidance (55%) and branching (24%) defects. Expression of Rac1Y40C.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4OK107 does not reduce the total percentage of axonal defects, but results in a marked shift in the distribution of defects, with most showing branching (45%) rather than guidance (31%) defects.