eye, with Scer\GAL4ey.PH
eye, with Scer\GAL4GMR.PF
The expression of p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PU leads to a decrease in eye size, as compared to controls.
Expression of p53Scer\UAS.Ex in the eye under the control of Scer\GAL4GMR.PF induces vast cell death and produces small and rough eyes with fused ommatidia.
Scer\GAL4Ilp2.PR-mediated, but not Scer\GAL4Sgs3.PD-mediated expression results in delayed pupation and a significant reduction in pupal volume compared to controls.
Expression of p53Scer\UAS.Ex in the developing eye, under the control of Scer\GAL4GMR.PF, causes a partial ablation of the eye due to excessive cell death during eye development.
Expression of p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PU results in a significant reduction in eye size and a disruption of ommatidial structure.
Scer\GAL4GMR.PU-mediated expression of p53Scer\UAS.Ex results in a disrupted adult eye, and increased apoptosis in the larval eye disc.
Expression of p53Scer\UAS.Ex under the control of Scer\GAL4insc-Mz1407 reduces neuroblast number by approximately 50%, compared to wild-type.
Overexpression of p53Scer\UAS.Ex in the developing eye under the control of Scer\GAL4GMR.PF generates a rough eye phenotype.
Expression of p53Scer\UAS.Ex under the control of Scer\GAL4hs.PU induces apoptosis in up to 18% of mitotically cycling imaginal disc cells, but not in any endocycling cells of salivary glands, fat body, or gut. Similar results are obtained in the ovary, where overexpression of p53 induces apoptosis in mitotically cycling but not endocycling follicle cells.
Expression of p53Scer\UAS.Ex under the control of Scer\GAL4ey.PH results in reduced eyes.
Expression of p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PF does not affect eye pigmentation levels.
Flies expressing p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PF have small eyes due to ectopic apoptosis.
Scer\GAL4GMR.PU, p53UAS.Ex has increased cell death phenotype, enhanceable by Hr3RA.UAS, Scer\GAL4GMR.PU
Scer\GAL4GMR.PU, p53UAS.Ex has increased cell death phenotype, enhanceable by Hr3RB.UAS, Scer\GAL4GMR.PU
Scer\GAL4GMR.PF, p53UAS.Ex has increased cell death phenotype, non-enhanceable by Df(3L)H99/Df(3L)XR38
Scer\GAL4GMR.PF, p53UAS.Ex has visible phenotype, non-enhanceable by Df(3L)H99/Df(3L)XR38
Scer\GAL4Ilp2.PR, p53UAS.Ex has decreased body size | pupal stage phenotype, suppressible | partially by Erk7KK102574, Scer\GAL4Ilp2.PR
Scer\GAL4Ilp2.PR, p53UAS.Ex has abnormal developmental rate phenotype, suppressible | partially by Erk7KK102574, Scer\GAL4Ilp2.PR
Scer\GAL4Ilp2.PR, p53UAS.Ex has decreased body size | pupal stage phenotype, suppressible | partially by Erk7HMS00222, Scer\GAL4Ilp2.PR
Scer\GAL4Ilp2.PR, p53UAS.Ex has abnormal developmental rate phenotype, suppressible | partially by Erk7HMS00222, Scer\GAL4Ilp2.PR
Scer\GAL4GMR.PU, p53UAS.Ex has visible phenotype, suppressible by SetUAS.cKa/Scer\GAL4GMR.PU
Scer\GAL4GMR.PU, p53UAS.Ex has abnormal size | adult stage phenotype, non-suppressible by Glyatc02982/Glyat[+]
Scer\GAL4GMR.PU, p53UAS.Ex has visible | adult stage phenotype, non-suppressible by Glyatc02982/Glyat[+]
Scer\GAL4GMR.PU, p53UAS.Ex has abnormal size | adult stage phenotype, non-suppressible by GlyatTH00482, Scer\GAL4GMR.PU
Scer\GAL4GMR.PU, p53UAS.Ex has visible | adult stage phenotype, non-suppressible by GlyatTH00482, Scer\GAL4GMR.PU
Scer\GAL4GMR.PF, p53UAS.Ex has increased cell death phenotype, non-suppressible by Df(3L)H99/Df(3L)XR38
Scer\GAL4GMR.PF, p53UAS.Ex has visible phenotype, non-suppressible by Df(3L)H99/Df(3L)XR38
p53UAS.Ex/Scer\GAL4ey.PH is a non-enhancer of increased cell death | larval stage | dominant phenotype of L2
Scer\GAL4insc-Mz1407, numbTS4D.UAS, p53UAS.Ex has increased cell death phenotype
Scer\GAL4GMR.PU, p53UAS.Ex has eye phenotype, enhanceable by Hr3RA.UAS, Scer\GAL4GMR.PU
Scer\GAL4GMR.PU, p53UAS.Ex has eye phenotype, enhanceable by Hr3RB.UAS, Scer\GAL4GMR.PU
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-enhanceable by Su(var)2-1003697/Su(var)2-10[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-enhanceable by lwr05486/lwr[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-enhanceable by Sumok06307/smt3[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-enhanceable by lwr05486/Sumok06307/smt3[+]/lwr[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-enhanceable by Scer\GAL4GMR.PF/SumoUAS.cPa
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-enhanceable by Df(3L)H99/Df(3L)XR38
Scer\GAL4GMR.PU, p53UAS.Ex has eye phenotype, suppressible by SetUAS.cKa/Scer\GAL4GMR.PU
Scer\GAL4insc-Mz1407, p53UAS.Ex has neuroblast phenotype, suppressible | partially by Scer\GAL4insc-Mz1407, agoΔF.UAS
Scer\GAL4insc-Mz1407, p53UAS.Ex has neuroblast phenotype, suppressible | partially by CycEUAS.cUa, Scer\GAL4insc-Mz1407
Scer\GAL4GMR.PU, p53UAS.Ex has eye phenotype, non-suppressible by Glyatc02982/Glyat[+]
Scer\GAL4GMR.PU, p53UAS.Ex has eye phenotype, non-suppressible by GlyatTH00482, Scer\GAL4GMR.PU
Scer\GAL4insc-Mz1407, p53UAS.Ex has neuroblast phenotype, non-suppressible by Scer\GAL4insc-Mz1407/BacA\p35UAS.cHa
Scer\GAL4insc-Mz1407, numbTS4D.UAS, p53UAS.Ex has neuroblast phenotype, non-suppressible by dapunspecified
Scer\GAL4insc-Mz1407, numbTS4D.UAS, p53UAS.Ex has neuroblast phenotype, non-suppressible by BacA\p35UAS.cHa, Scer\GAL4insc-Mz1407
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-suppressible by Scer\GAL4GMR.PF/SumoUAS.cPa
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-suppressible by Su(var)2-1003697/Su(var)2-10[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-suppressible by lwr05486/lwr[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-suppressible by Sumok06307/smt3[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-suppressible by lwr05486/Sumok06307/smt3[+]/lwr[+]
Scer\GAL4GMR.PF, p53UAS.Ex has eye phenotype, non-suppressible by Df(3L)H99/Df(3L)XR38
p53UAS.Ex/Scer\GAL4ey.PH is a non-enhancer of eye disc | ventral phenotype of L2
p53UAS.Ex/Scer\GAL4ey.PH is a non-enhancer of eye | ventral phenotype of L2
Scer\GAL4insc-Mz1407/p53UAS.Ex is a suppressor of neuroblast | increased number phenotype of Scer\GAL4insc-Mz1407, numbTS4D.UAS
Scer\GAL4insc-Mz1407/p53UAS.Ex is a suppressor of neuroblast | increased number | somatic clone phenotype of numb15
Scer\GAL4VP16.nanos.UTR/p53UAS.Ex is a suppressor | partially of primordial germ cell phenotype of out2
Scer\GAL4insc-Mz1407, p53UAS.Ex, CycEUAS.cUa is a non-suppressor of neuroblast | increased number | somatic clone phenotype of numb15
The small eye phenotype resulting from the expression of p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PU is not suppressed by heterozygosity for Glyatc02982 or by the co-expression of GlyatTH00482.
A Cdk7S164A.T170A mutant background significantly suppresses the partial eye ablation found upon expression of p53Scer\UAS.Ex in the developing eye, under the control of Scer\GAL4GMR.PF.
Co-expression of SetScer\UAS.cKa significantly suppresses the eye defects caused by expression of p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PU.
Co-expression of Hr46RA.Scer\UAS or Hr46RB.Scer\UAS enhances the degenerative eye phenotype caused by Scer\GAL4GMR.PU-mediated expression of p53Scer\UAS.Ex.
Co-expression of Hr46RA.Scer\UAS or Hr46RB.Scer\UAS results in highly increased cell death in eye discs compared to Scer\GAL4GMR.PU-mediated expression of p53Scer\UAS.Ex alone.
Expression of p53Scer\UAS.Ex in numb15 mutant clones under the control of Scer\GAL4insc-Mz1407 effectively inhibits 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.
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 agoΔF.Scer\UAS or CycEScer\UAS.cUa can partially suppress the neuroblast-loss phenotype induced by overexpression of p53Scer\UAS.Ex under the control of Scer\GAL4insc-Mz1407.
Co-expression of CycEScer\UAS.cUa and p53Scer\UAS.Ex generates a significant increase in ectopic neuroblasts in a numb15 mutant background, compared to overexpression of p53Scer\UAS.Ex alone in a numb15 mutant background.
The rough eye phenotype found at 29[o]C in flies expressing p53Scer\UAS.Ex under the control of Scer\GAL4GMR.PF is not affected by a Su(var)2-1003697, lwr05486, or smt3k06307 heterozygous background nor in a lwr05486-smt3k06307 transheterozygous background.
Co-expression of smt3Scer\UAS.cPa with p53Scer\UAS.Ex in the developing eye at 25[o]C or 29[o]C, under the control of Scer\GAL4GMR.PF does not affect the p53Scer\UAS.Ex-related rough eye phenotype.
The defective programmed cell death of the primordial germ cells (PGCs) see in out1 homozygous embryos is partially rescued by expression of p53Scer\UAS.Ex under the control of Scer\GAL4nos.UTR.T:Hsim\VP16.
Expression of p53Scer\UAS.Ex under the control of Scer\GAL4ey.PH does not enhance the L2/+ mutant phenotype of ventral eye loss.
The presence of p53Scer\UAS.Ex, under the control of Scer\GAL4GMR.PF does not affect the reduction in eye pigmentation observed in Ada2bd842 heterozygotes.
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).
Co-expression of BacA\p35Scer\UAS.cHa does not affect the suppression of ectopic neuroblast formation by p53Scer\UAS.Ex (both transgenes under the control of Scer\GAL4insc-Mz1407) in numb15 mutant neuroblast clones.