Pfdn201239/Df(3L)BSC457 mutants show ectopic neuroblasts in third instar larval brains and an increase in the number of cells in S-phase (assessed by EdU labelling).They also display defects in asymmetric protein segregation (both in metaphase and telophase) and mitotic spindle orientation in neuroblasts.
Pfdn2Δ10/Pfdn201239 transheterozygotes display increased average number of brain neuroblasts compared to wild-type.
Pfdn2Δ10/Pfdn201239 has abnormal neuroanatomy | third instar larval stage phenotype, suppressible | partially by aPKCGD1366/Scer\GAL4insc-Mz1407
Pfdn2Δ10/Pfdn201239 has increased cell number | third instar larval stage phenotype, suppressible | partially by aPKCGD1366/Scer\GAL4insc-Mz1407
Pfdn2Δ10/Pfdn201239 has abnormal neuroanatomy | third instar larval stage phenotype, suppressible | partially by par-6GD4048/Scer\GAL4insc-Mz1407
Pfdn2Δ10/Pfdn201239 has increased cell number | third instar larval stage phenotype, suppressible | partially by par-6GD4048/Scer\GAL4insc-Mz1407
Pfdn2Δ10/Pfdn201239 has neuroblast | increased number | third instar larval stage phenotype, suppressible | partially by aPKCGD1366/Scer\GAL4insc-Mz1407
Pfdn2Δ10/Pfdn201239 has neuroblast | increased number | third instar larval stage phenotype, suppressible | partially by par-6GD4048/Scer\GAL4insc-Mz1407
The dramatically increased average number of brain neuroblasts characteristic for Pfdn2Δ10/Pfdn201239 transheterozygote third instar larvae is partially restored by expression of either aPKCGD1366 or par-6GD4048 under the control of Scer\GAL4insc-Mz1407 in the mutant background.
A. Spradling.
Complements: SuURES.
Complements: l(3)0369103691. Complements: klu09036. Complements: klu10052.