Amino acid replacement: L788term.
T7947596A
L788term | Ubr3-PB; L788term | Ubr3-PC; L788term | Ubr3-PA
L788term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Pupae with Ubr3B mutant clones in the Johnston's organ exhibit scolopidia detached from the hinge of the second and third antennal segment and in adulthood display significant reduction in the sound evoked potentials in electroantennogram measurements.
Ubr3B has abnormal neuroanatomy | P-stage | somatic clone phenotype, enhanceable | somatic clone by Scer\GAL4Act.PU/ckUAS.GFP
Ubr3B has abnormal developmental rate | somatic clone phenotype, suppressible by Scer\GAL4Act.PU/cosKK106270
Ubr3B has increased cell death | somatic clone phenotype, suppressible by Scer\GAL4Act.PU/BacA\p35UAS.cUa
Ubr3B has abnormal developmental rate | somatic clone phenotype, non-suppressible by Scer\GAL4Act.PU/BacA\p35UAS.cUa
Ubr3B has Johnston organ | P-stage | somatic clone phenotype, enhanceable | somatic clone by Scer\GAL4Act.PU/ckUAS.GFP
Ubr3B has scolopidium | P-stage | somatic clone phenotype, enhanceable | somatic clone by Scer\GAL4Act.PU/ckUAS.GFP
Ubr3B has Johnston organ | P-stage | somatic clone phenotype, enhanceable by Sans245/Sans[+]
Ubr3B has scolopidium | P-stage | somatic clone phenotype, enhanceable by Sans245/Sans[+]
Ubr3B has Johnston organ | P-stage | somatic clone phenotype, enhanceable by Cad99C57A/Cad99C[+]
Ubr3B has scolopidium | P-stage | somatic clone phenotype, enhanceable by Cad99C57A/Cad99C[+]
Ubr3B has photoreceptor neuron | somatic clone phenotype, suppressible by Scer\GAL4Act.PU/cosKK106270
Ubr3B has photoreceptor neuron | somatic clone phenotype, non-suppressible by Scer\GAL4Act.PU/BacA\p35UAS.cUa
Ubr3B/Ubr3B is a non-enhancer | somatic clone of Johnston organ | P-stage | somatic clone phenotype of Scer\GAL4Act.PU, ckGD1408
Ubr3B/Ubr3B is a non-enhancer | somatic clone of scolopidium | P-stage | somatic clone phenotype of Scer\GAL4Act.PU, ckGD1408
Expression of cosKK106270 under the control of Scer\GAL4Act.PU rescues the delayed photoreceptor differentiation phenotype of Ubr3B/Ubr3B mutant clones.
The scolopidia detachment phenotype observed in Ubr3B mutant clones in the pupal Johnston's organ is significantly enhanced by expression of ckScer\UAS.T:Avic\GFP under the control of Scer\GAL4Act.PU in the mutant cells or by combination with a single copy of either Sans245 or Cad99C57A.
Flies carrying Ubr3B mutant clones expressing (under the Scer\GAL4Act.PU driver) ckGD1408 in the Johnston's organ display nearly complete detachment of scolopidia from the hinge of the second and third antennal segment - similar to animals with clones expressing the ckGD1408 alone.
Expression of BacA\p35Scer\UAS.cUa under the control of Scer\GAL4Act.PU suppresses the apoptosis phenotype, but fails to rescue the delayed photoreceptor differentiation phenotype of Ubr3B/Ubr3B mutant clones.
Ubr3B is rescued by Ubr3+t18.3
Ubr3B is rescued by Scer\GAL4Act.PU/Ubr3UAS.cLa
Ubr3B is rescued by Scer\GAL4Act.PU/Ubr3UAS.cLa.Tag:FLAG
Ubr3B is not rescued by Scer\GAL4Act.PU/Ubr3RINGmut.UAS.Tag:FLAG
Ubr3B fails to complement the lethality of Ubr3G0307a.
Ubr3+t18.3 fully rescues the lethality of Ubr3B hemizygous mutants.
The sound transduction defects (reduced amplitude of sound evoked potentials) observed in adult flies carrying Ubr3B mutant clones in the Johnston's organ can be rescued by expression of Ubr3Scer\UAS.cLa driven by Scer\GAL4Act.PU in the mutant cells.
The detached scolopidia phenotype observed in pupae bearing Ubr3B mutant clones in the Johnston's organ can be rescued by expression of Ubr3[Scer\UAS.cLa. T:Zzzz \FLAG] (but not Ubr3RINGmut.Scer\UAS.T:Zzzz\FLAG) driven by Scer\GAL4Act.PU in the mutant cells.