Overexpression of numbS2D.Scer\UAS in larval brain neuroblasts under the control of Scer\GAL4insc-Mz1407 leads to a significant increase in type II neuroblast number.
Expression of numbS2D.Scer\UAS under the control of Scer\GAL4insc-Mz1407 induces a mild supernumerary neuroblast phenotype.
Scer\GAL4insc-Mz1407, numbS2D.UAS has abnormal neuroanatomy phenotype, enhanceable by DroncRNAi.UAS.Ka, Scer\GAL4insc-Mz1407
Scer\GAL4insc-Mz1407, numbS2D.UAS has abnormal neuroanatomy phenotype, enhanceable by Dronc51
Scer\GAL4insc-Mz1407, numbS2D.UAS has neuroblast phenotype, enhanceable by DroncRNAi.UAS.Ka, Scer\GAL4insc-Mz1407
Scer\GAL4insc-Mz1407, numbS2D.UAS has type II neuroblast | increased number phenotype, enhanceable by DroncRNAi.UAS.Ka, Scer\GAL4insc-Mz1407
Scer\GAL4insc-Mz1407, numbS2D.UAS has neuroblast phenotype, enhanceable by Dronc51
Scer\GAL4insc-Mz1407, numbS2D.UAS has type II neuroblast | increased number phenotype, enhanceable by Dronc51
Knockdown of Nc through expression of NcdsRNA.Scer\UAS significantly augmented numbS2D.Scer\UAS induced ectopic neuroblast formation. This enhancement is not due to prevention of neuroblast apoptosis, as the total number of TUNEL[+] cells in the central brain doesn't change.
A Nc51 heterozygous background enhances ectopic neuroblast formation due to numbS2D.Scer\UAS expression.
?p53[-] p2.