Imprecise excision of the progenitor insertion, resulting in a deletion that removes 291bp of debcl, including a portion of the promoter region and transcriptional start site.
Homozygous debclE26 mutant larvae do not display any NMJ degeneration or changes in NMJ morphology.
The survival of glial cells within notal microchaete clusters in debclE26 mutants is similar to wild type.
Mutants are viable with no overt mutant adult phenotypes.
The distribution and number of apoptotic cells is similar to that of control embryos in mutant stage 11 and late stage 12 embryos.
Stage 16 mutant embryos have normal central and peripheral nervous system patterning and no fusion of commissural axon bundles is seen.
Normal histolysis of the larval midgut occurs during pupation in the mutant animals and larval salivary glands also undergo histolysis. Programmed cell death in the pupal retina also occurs normally to remove a subset of interommatidial cells. Programmed cell death in the arista is also normal in the mutants.
The pattern of mitotic cells in the developing mutant embryo is normal.
Mutant adults are not susceptible to infection by E.coli (infection by pricking with a needle dipped in a concentrated pellet of E.coli).
The apoptotic response to irradiation is significantly decreased in mutant embryos compared to wild type.
Debcl[+]/DebclE26 is a non-enhancer of visible phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
Buffy[+], Debcl[+], DebclE26, BuffyH37 is a non-enhancer of visible phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
Debcl[+]/DebclE26 is a non-enhancer of visible | adult stage phenotype of HPV18\E6UAS.Tag:MYC, Hsap\UBE3AUAS.cRa, Scer\GAL4GMR.PU
DebclE26 is a suppressor | partially of abnormal neuroanatomy phenotype of Ank2f02001
Debcl[+]/DebclE26 is a non-suppressor of visible phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
Buffy[+], Debcl[+], DebclE26, BuffyH37 is a non-suppressor of visible phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
DebclE26 is a non-suppressor of increased cell death phenotype of grimGMR.PC
Debcl[+]/DebclE26 is a non-enhancer of eye phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
Buffy[+], Debcl[+], DebclE26, BuffyH37 is a non-enhancer of eye phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
Debcl[+]/DebclE26 is a non-enhancer of eye phenotype of HPV18\E6UAS.Tag:MYC, Hsap\UBE3AUAS.cRa, Scer\GAL4GMR.PU
DebclE26 is a suppressor | partially of embryonic/larval neuromuscular junction phenotype of Ank2f02001
Debcl[+]/DebclE26 is a non-suppressor of eye phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
Buffy[+], Debcl[+], DebclE26, BuffyH37 is a non-suppressor of eye phenotype of Hsap\BCL2L13UAS.cNa, Scer\GAL4GMR.PS
DebclE26 is a non-suppressor of eye phenotype of grimGMR.PC
Homozygous debclE26 partially suppresses the NMJ degeneration seen in Ank2f02001 mutants.
The cell death seen in grimGMR.PC eyes is not abrogated in a debclE26 background.
debclE26 BuffyH37 double mutants are viable with no overt mutant adult phenotypes.
The distribution and number of apoptotic cells is similar to that of control embryos in debclE26 BuffyH37 double mutant stage 11 and late stage 12 embryos. Stage 16 double mutant embryos have normal central and peripheral nervous system patterning and no fusion of commissural axon bundles is seen. Normal histolysis of the larval midgut occurs during pupation in the double mutant animals and larval salivary glands also undergo histolysis. Programmed cell death in the pupal retina also occurs normally to remove a subset of interommatidial cells. Programmed cell death in the arista is also normal in the double mutants.
The pattern of mitotic cells in the developing debclE26 BuffyH37 double mutant embryo is normal.
debclE26 BuffyH37 double adults are not susceptible to infection by E.coli (infection by pricking with a needle dipped in a concentrated pellet of E.coli).
The apoptotic response to irradiation is increased in debclE26 BuffyH37 double mutant embryos compared to wild type.
The rough eye phenotype induced by expression of Hsap\BCL2L13Scer\UAS.cNa driven by Scer\GAL4GMR.PS is not significantly enhanced or suppressed by DebclE26/+ or DebclE26 BuffyH37/+. DebclE26/+ or DebclE26 BuffyH37/+ does not result in significant eye phenotypes in Scer\GAL4GMR.PS>Hsap\BCL2L13ΔTM.Scer\UAS flies.
Heterozygosity for DebclE26 does not modify the fully penetrant rough eye phenotype resulting from the co-expression of HPV18\E6Scer\UAS.T:Hsap\MYC and Hsap\UBE3AScer\UAS.cRa under the control of Scer\GAL4GMR.PU, leading to severe eye necrosis.