Generated through imprecise excision of P{PZ}S6k07084 resulting in Df(3)07084 with a deletion of 3150bp, removing the last 180bp of mad2, all of gene CG5537 and the first 1120bp of S6k.
mad2Δ dividing cells in third instar larval brains rarely exhibit aneuploidy and do not show any increase in apoptosis. However, the aneuploid cells are qualitatively different from those of wild-type, with almost all being polyploids, suggesting a rare complete failure of segregation.
mad2Δ mutants do not show accumulation of mitotic cells in colchicine-treated larval brains.
There are no obvious aberrations in chromosome behaviour in mad2Δ mutants compared to controls. Mitosis appears to function normally in mad2Δ cells although anaphase onset is accelerated in mad2Δ mutant neuroblasts. The time from nuclear envelope breakdown to the onset of CycB degradation is substantially reduced in mad2Δ mutants. The average time required to degrade spindle-associated CycB and initiate anaphase in mad2Δ cells is longer than the average time for achieving alignment of kinetochores on the metaphase place.
mad2Δ is a suppressor of abnormal mitotic cell cycle | larval stage phenotype of aspE3