leg (with DCP2BG01766)
ommatidium (with DCP2BG01766)
wing (with DCP2BG01766)
wing disc | larval stage (with DCP2BG01766)
wing disc | larval stage (with DCP2e00034)
DCP2tb homozygotes exhibit bloating and cessation of growth at P-stage.
DCP2tb homozygous third instar larvae exhibit gross morphological alterations in the size of larval brain, wing, eye and leg discs in the early and late larval phase. They also exhibit an increased occurrence of cell division in larval brains and wing discs; progressive loss of mature neurons in larval brains and eye discs; and an enlargement of leg discs in size. During late larval phase, eye discs exhibit deviations from the usual regular arrangement of ommatidia.
DCP2tb/DCP2tb or DCP2tb/DCP2e00034 larval brains exhibit increased occurrence of cell division.
DCP2tb homozygous larvae exhibit an increase in cell number concomitant with a decrease in cell size in wing discs and an increase in cell number in optic lobe.
DCP2BG01766/DCP2tb adults exhibit several developmental abnormalities: defects in thorax closure; loss of abdominal para-segments, abdominal bristles and regular arrangement of ommatidia; and presence of abnormal external male genitalia.
Pupation is delayed and the mutant larvae form pupae but ultimately die. Brain optic lobes are enlarged and the wing imaginal discs show abnormal folding with protrusion of the pouch region. A progressive increase in mitotically active cells with abnormal chromosome condensation is observed with the progression of tumorigenesis.
DCP2tb is partially rescued by DCP2UAS.cRa/Scer\GAL4Act5C.PI
DCP2tb is partially rescued by DCP2UAS.cRa/Scer\GAL4Tub.PU
Isolated as a second-site mutation in a P-element mutagenesis screen.