Two deletions remove a 1314bp and a 593bp segment that includes the minimal promoter and 5' transcribed leader sequence.
nerfin-1159/Df(3L)Exel6086 embryos show strongly disorganized Fas2-immunopositive fascicles and disorganized or absent ap-expressing axons, despite having a similar number of ap-expressing neurons as controls.
Larval optic lobe nerfin-1159/nerfin-1159 mutant clones include ectopic neuroblasts, located where post-mitotic neurons should be. These neuroblasts exhibit proliferation potential as shown by an increase in the number of mitotic cells in these clones, and form tumors at the adult stage. Medulla neurons are generated normally, but soon begin to de-differentiate, suggesting that the origin of these ectopic neuroblasts is de-differentiation of neurons. The number of GMCs does not significantly change in nerfin-1159/nerfin-1159 mutant clones.
nerfin-1159 has neoplasia | somatic clone | adult stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/NKK102890
nerfin-1159 has abnormal neuroanatomy | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/NKK102890
nerfin-1159 has abnormal neuroanatomy | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/DeltaGL00520
nerfin-1159 has abnormal neuroanatomy | somatic clone | larval stage phenotype, non-suppressible | somatic clone by MycKK103869/Scer\GAL4Tub.PU
nerfin-1159 has abnormal neuroanatomy | somatic clone | larval stage phenotype, non-suppressible | somatic clone by Scer\GAL4Tub.PU/mTorTED.UAS
nerfin-1159/nerfin-1[+] is a suppressor | partially | somatic clone of abnormal neuroanatomy | somatic clone | adult stage phenotype of prosIG2227
nerfin-1159 has neuroblast | ectopic | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/NKK102890
nerfin-1159 has adult optic lobe | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/NKK102890
nerfin-1159 has neuroblast | ectopic | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/DeltaGL00520
nerfin-1159 has adult optic lobe | somatic clone | larval stage phenotype, suppressible | somatic clone by Scer\GAL4Tub.PU/DeltaGL00520
nerfin-1159 has neuroblast | ectopic | somatic clone | larval stage phenotype, non-suppressible | somatic clone by MycKK103869/Scer\GAL4Tub.PU
nerfin-1159 has adult optic lobe | somatic clone | larval stage phenotype, non-suppressible | somatic clone by MycKK103869/Scer\GAL4Tub.PU
nerfin-1159 has neuroblast | ectopic | somatic clone | larval stage phenotype, non-suppressible | somatic clone by Scer\GAL4Tub.PU/mTorTED.UAS
nerfin-1159 has adult optic lobe | somatic clone | larval stage phenotype, non-suppressible | somatic clone by Scer\GAL4Tub.PU/mTorTED.UAS
nerfin-1159/nerfin-1[+] is a suppressor | partially | somatic clone of carbon dioxide sensitive neuron | ectopic | somatic clone phenotype of prosIG2227
Clonal expression of NKK102890 or DlGL00520 (but not MycKK103869 or TorTED.Scer\UAS) under the control of Scer\GAL4tub.PU, largely suppresses the formation of ectopic neuroblasts in larval optic lobe nerfin-1159/nerfin-1159 mutant clones; and expression of NKK102890 suppresses tumor formation at the adult stage in these clones.
The number of ectopic CO[[2]] neurons on the maxillary palp in animals containing prosIG2227 clones is significantly suppressed if they are also carrying nerfin-1159/+.
nerfin-1159 is rescued by Scer\GAL4Tub.PU/nerfin-1UAS.cXa
nerfin-1159 is partially rescued by Scer\GAL4Tub.PU/nerfin-1dZF3.UAS
nerfin-1159 is not rescued by nerfin-1dZF1.UAS/Scer\GAL4Tub.PU
nerfin-1159 is not rescued by Scer\GAL4Tub.PU/nerfin-1dZF2.UAS
Expression of nerfin-1dZF3.Scer\UAS or nerfin-1Scer\UAS.cXa (but not nerfin-1dZF1.Scer\UAS or nerfin-1dZF2.Scer\UAS) under the control of Scer\GAL4tub.PU substantially decreases the number of ectopic neuroblasts in nerfin-1159/nerfin-1159 mutant clones.
Created as a consequence of the "ends in" homologous recombination gene knockout technique. The deletion was most likely caused by exonuclease digestion of the targeting vector after the SceI exonuclease induced double strand break but before its integration into the nerfin-1 chromosomal locus. The deletion was detected after the allelic substitution step and are most likely the result of illegitimate recombination between micro-homologies present in the minimal promoter of one copy of the nerfin-1 duplication and the transcribed region of the tandem copy.