UASt regulatory sequences drive expression of an inverted repeat.
Expression of αTub84BGD17779 (together with UAS-Dicer2 to enhance RNAi efficiency) under the control of Scer\GAL4insc-Mz1407 results in formation of ectopic neuroblast in both type I lineages and type II lineages in third instar larval brains.
Expression of αTub84BGD17779 under the control of Scer\GAL4erm.PU does not have any obvious effect on neuroblast numbers in third instar larval brains compared to controls.
αTub84BGD17779, Scer\GAL4insc-Mz1407 has abnormal neuroanatomy | third instar larval stage phenotype, enhanceable by pinsP89
αTub84BGD17779, Scer\GAL4insc-Mz1407 has increased cell number | third instar larval stage phenotype, enhanceable by pinsP89
Scer\GAL4insc-Mz1407/αTub84BGD17779 is a suppressor of abnormal neuroanatomy | third instar larval stage phenotype of pinsP89
Scer\GAL4insc-Mz1407/αTub84BGD17779 is a suppressor of decreased cell number | third instar larval stage phenotype of pinsP89
αTub84BGD17779, Scer\GAL4insc-Mz1407 has type I neuroblast | third instar larval stage | increased number phenotype, enhanceable by pinsP89
αTub84BGD17779, Scer\GAL4insc-Mz1407 has type II neuroblast | third instar larval stage | increased number phenotype, enhanceable by pinsP89
αTub84BGD17779, Scer\GAL4GMR.PF is an enhancer of eye phenotype of Hsap\MAPTR406W.UAS, Scer\GAL4GMR.PF
αTub84BGD17779, Scer\GAL4GMR.PF is a non-enhancer of eye phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
αTub84BGD17779, Scer\GAL4GMR.PF is a non-suppressor of eye phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
The increased number of brain neuroblasts observed in third instar larvae expressing αTub84BGD17779 under the control of Scer\GAL4insc-Mz1407 is increased further by combination with pinsP89 (although the pinsP89 mutants on their own display significantly lower number of brain neuroblasts compared to controls) and leads to a dramatic neuroblast overgrowth.
Expression of αTub84BGD17779 under the control of Scer\GAL4erm.PU in pinsP89 mutant background leads to severely increased number of neuroblast due to dedifferentiation of intermediate neural progenitors.