Cul1k01207 mutant clones in sensory neurons in adult wing do not display any defects in injury-induced axon degeneration (following an axotomy, the severed axons are cleared away normally).
Mutant embryos cultured under hypoxic conditions (5% O[[2]]) show increased eclosion compared to controls raised under the same conditions.
lin19k01207 mutant C4da neuron clones exhibit an increase in cell death and die during early metamorphosis.
Females carrying lin19k01207 germ line clones generated using the FLP-FRT ovoD1 method, never lay any eggs. Oogenesis in these flies arrests during the early stages, sometimes producing highly polyploid, one-cell cysts.
No defects are seen in axon pruning during metamorphosis, though a slight proliferation defect is seen when somatic clones are made in the neuroblast.
Cul1k01207 is a non-suppressor of abnormal neuroanatomy | somatic clone | adult stage phenotype of SarmΔARM.UAS.Tag:MYC, Scer\GAL4VGlut1-OK371
CSN4unspecified, Cul1k01207 has increased cell death | oogenesis phenotype
CSN4unspecified, Cul1k01207 has abnormal cell number | oogenesis phenotype
Cul1k01207/Cul1[+] is an enhancer of wing phenotype of Mmus\Cul1UAS.cHa, Scer\GAL4Bx-MS1096
Cul1k01207 is a non-suppressor of sensory neuron | somatic clone | adult stage phenotype of SarmΔARM.UAS.Tag:MYC, Scer\GAL4VGlut1-OK371
Cul1k01207 is a non-suppressor of axon | somatic clone | adult stage phenotype of SarmΔARM.UAS.Tag:MYC, Scer\GAL4VGlut1-OK371
CSN5unspecified, Cul1k01207 has ovary phenotype
CSN5unspecified, Cul1k01207 has nurse cell phenotype
CSN4unspecified/CSN4[+], Cul1k01207 has nurse cell phenotype
CSN4unspecified/CSN4[+], Cul1k01207 has stalk follicle cell phenotype
CSN5[+]/CSN5unspecified, Cul1k01207 has ovary phenotype
CSN5[+]/CSN5unspecified, Cul1k01207 has nurse cell phenotype
CSN5[+]/CSN5unspecified, Cul1k01207 has stalk follicle cell phenotype
CSN4unspecified, Cul1k01207 has ovary phenotype
CSN4unspecified, Cul1k01207 has nurse cell phenotype
CSN4unspecified, Cul1k01207 has stalk follicle cell phenotype
CSN4unspecified, lin19[+]/Cul1k01207 has ovary phenotype
CSN4unspecified, lin19[+]/Cul1k01207 has nurse cell phenotype
CSN5unspecified, Cul1k01207 has stalk follicle cell phenotype
CSN4unspecified, lin19[+]/Cul1k01207 has stalk follicle cell phenotype
CSN5unspecified, lin19[+]/Cul1k01207 has ovary phenotype
CSN5unspecified, lin19[+]/Cul1k01207 has nurse cell phenotype
CSN5unspecified, lin19[+]/Cul1k01207 has stalk follicle cell phenotype
CSN4unspecified/CSN4[+], Cul1k01207 has ovary phenotype
The axon degeneration in sensory neurons clones in the adult wing expressing Ect4ΔARM.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4VGlut-OK371 can be suppressed by combination with Cul1k01207.
Unlike either single heterozygote, ovaries from CSN4unspecified; lin19k01207 or CSN5unspecified; lin19k01207 transheterozygous females display various defects: cell death, abnormal number of nurse cells per egg chamber, and loss of stalk cells.
Introduction of a single copy of Cul1k01207 or Df(2R)NCX8 dominantly enhances the wing reduction phenotype in Mmus\Cul1Scer\UAS.cHa Scer\GAL4Bx-MS1096 mutants.
I. Kiss.
Complements: l(2)0849208492. Complements: rnh1k07409a. Complements: hrgk07619. Complements: rnh1k07624.