Larval brain clones expressing numbTS4D.Scer\UAS under the control of Scer\GAL4Act.PU exhibit ectopic type II neuroblasts.
Overexpression of numbTS4D.Scer\UAS in larval brain neuroblasts under the control of Scer\GAL4insc-Mz1407 leads to a very dramatic increase in type II neuroblast number (compared to expression of numbS2D.Scer\UAS). While neuroblasts are more proliferative in these mutants, the number of elav-positive postmitotic neurons. numb localisation into basal crescents in these neuroblasts appears normal, although some show compromised localisation at metaphase and telophase.
Expression of numbTS4D.Scer\UAS in the type-I neuroblast lineage under the control of Scer\GAL4ase.neuro has no effect on neuroblast number.
Scer\GAL4erm.R9D11-driven expression of numbTS4D.Scer\UAS in mature INPs, GMCs, and differentiated neurons fails to induce ectopic neuroblast formation.
Type-II neuroblasts clones expressing numbTS4D.Scer\UAS contain ectopic neuroblasts, whereas numbTS4D.Scer\UAS-expressing type-I neuroblast clones always contain a single neuroblast, as found in controls.
Expression of numbTS4D.Scer\UAS under the control of Scer\GAL4insc-Mz1407 induces supernumerary neuroblast formation.
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, enhanceable by Scer\GAL4insc-Mz1407/DroncΔN.UAS
Scer\GAL4Act.PU, numbTS4D.UAS has increased cell number | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Act.PU/mir-bansponge.UAS.DsRed(Unk)
Scer\GAL4Act.PU, numbTS4D.UAS has abnormal neuroanatomy | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Act.PU/mir-bansponge.UAS.DsRed(Unk)
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, suppressible by Scer\GAL4insc-Mz1407, numbTS4D.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, suppressible by Scer\GAL4insc-Mz1407/DroncΔN.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, suppressible by spdoG104
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, suppressible by Nl1N-ts1
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, suppressible by NGD144, Scer\GAL4insc-Mz1407
Scer\GAL4Act.PU, numbTS4D.UAS has increased cell number | somatic clone | larval stage phenotype, non-suppressible | somatic clone by Scer\GAL4Act.PU/mir-banD.UAS.EGFP
Scer\GAL4Act.PU, numbTS4D.UAS has abnormal neuroanatomy | somatic clone | larval stage phenotype, non-suppressible | somatic clone by Scer\GAL4Act.PU/mir-banD.UAS.EGFP
Scer\GAL4insc-Mz1407, numbTS4D.UAS has abnormal neuroanatomy phenotype, non-suppressible by Scer\GAL4insc-Mz1407/ponS611D.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS is a suppressor of abnormal neuroanatomy phenotype of Scer\GAL4insc-Mz1407, numbTS4D.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS, p53UAS.Ex has increased cell death phenotype
Scer\GAL4insc-Mz1407, numbTS4D.UAS has neuron | increased number phenotype, enhanceable by Scer\GAL4insc-Mz1407/DroncΔN.UAS
Scer\GAL4Act.PU, numbTS4D.UAS has type II neuroblast | increased number | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Act.PU/mir-bansponge.UAS.DsRed(Unk)
Scer\GAL4insc-Mz1407, numbTS4D.UAS has type II neuroblast | increased number phenotype, suppressible by Scer\GAL4insc-Mz1407/DroncΔN.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS has type II neuroblast | increased number phenotype, suppressible by spdoG104
Scer\GAL4insc-Mz1407, numbTS4D.UAS has type II neuroblast | increased number phenotype, suppressible by Nl1N-ts1
Scer\GAL4insc-Mz1407, numbTS4D.UAS has type II neuroblast | increased number phenotype, suppressible by NGD144, Scer\GAL4insc-Mz1407
Scer\GAL4insc-Mz1407, numbTS4D.UAS has type II neuroblast | increased number phenotype, suppressible by Scer\GAL4insc-Mz1407, numbTS4D.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS has neuroblast | increased number phenotype, suppressible by Scer\GAL4insc-Mz1407/p53UAS.Ex
Scer\GAL4Act.PU, numbTS4D.UAS has type II neuroblast | increased number | somatic clone | larval stage phenotype, non-suppressible | somatic clone by Scer\GAL4Act.PU/mir-banD.UAS.EGFP
Scer\GAL4insc-Mz1407, numbTS4D.UAS has type II neuroblast | increased number phenotype, non-suppressible by Scer\GAL4insc-Mz1407/ponS611D.UAS
Scer\GAL4insc-Mz1407, numbTS4D.UAS, p53UAS.Ex has neuroblast phenotype, non-suppressible by dapunspecified
Scer\GAL4insc-Mz1407, numbTS4D.UAS has neuroblast | increased number phenotype, non-suppressible by Scer\GAL4insc-Mz1407/p53H159N.UAS.Ex
Scer\GAL4insc-Mz1407, numbTS4D.UAS, p53UAS.Ex has neuroblast phenotype, non-suppressible by BacA\p35UAS.cHa, Scer\GAL4insc-Mz1407
Scer\GAL4insc-Mz1407, numbTS4D.UAS is a suppressor of type II neuroblast | increased number phenotype of Scer\GAL4insc-Mz1407, numbTS4D.UAS
Co-expression of bansponge.Scer\UAS.T:Disc\RFP, but not banD.Scer\UAS.T:Avic\GFP-EGFP, suppresses the ectopic type II neuroblast phenotype seen in larval brain clones expressing numbTS4D.Scer\UAS under the control of Scer\GAL4Act.PU.
Expression of Ncpro.Scer\UAS attenuates numbTS4D.Scer\UAS induced ectopic neuroblast formation.
Expression of NcΔN.Scer\UAS attenuates numbTS4D.Scer\UAS induced ectopic neuroblast formation. No change in apoptosis is reported in this background, although the number of postmitotic neurons is increased.
Co-expression of ponS611D.Scer\UAS under the control of Scer\GAL4insc-Mz1407 rescues numbTS4D.Scer\UAS localisation at metaphase and telophase, but is unable to rescue ectopic type II neuroblast formation.
numbTS4D.Scer\UAS induced ectopic neuroblast formation is abolished in spdoG104 mutant clones.
Inhibition of N activity through Nl1N-ts1 suppresses numbTS4D.Scer\UAS induced ectopic neuroblast formation.
Inhibition of N activity through NGD144 suppresses numbTS4D.Scer\UAS induced ectopic neuroblast formation.
Co-expression of p53Scer\UAS.Ex suppresses ectopic neuroblast formation induced by numbTS4D.Scer\UAS expression under the control of Scer\GAL4insc-Mz1407.
Co-expression of p53H159N.Scer\UAS.Ex (that lacks transactivation activity) does not suppress supernumerary neuroblast formation induced by numbTS4D.Scer\UAS expression under the control of Scer\GAL4insc-Mz1407.
Larval brains expressing numbTS4D.Scer\UAS and p53Scer\UAS.Ex under the control of Scer\GAL4insc-Mz1407 exhibit an overall increase in apoptosis compared to controls (as visualised by TUNEL). However, neuroblast apoptosis remains rare, indicating that the apoptosis increase is in post-mitotic neurons or other brain cells.
A dapunspecified mutant background does not attenuate the ability of p53Scer\UAS.Ex expression to suppress the formation of ectopic neuroblasts induced by numbTS4D.Scer\UAS expression (under the control of Scer\GAL4insc-Mz1407).
Co-expression of BacA\p35Scer\UAS.cHa does not affect the suppression of ectopic neuroblast formation by p53Scer\UAS.Ex in numbTS4D.Scer\UAS-expressing larval brains (all transgenes under the control of Scer\GAL4insc-Mz1407).
Scer\GAL4insc-Mz1407/numbTS4D.UAS fails to rescue numb15
Expression of numbTS4D.Scer\UAS fails to suppress the ectopic neuroblast formation seen in numb15 mutant clones.