JhI-1ED24 mutant somatic clones induced in JhI-1ΔMTS.T:SV5\V5 expressing background are significantly smaller than their twin spot clone in third instar larval eye discs and clones located posterior of the morphogenetic furrow where a band of cells synchronously enter the final round of mitosis show fewer cells in the S-phase and no cells in the M-phase of the mitotic cycle.
JhI-1ED24;JhI-1ΔMTS.T:SV5\V5 mutant cells derived from JhI-1ED24 homozygous mutant somatic clones induced in wing discs carrying the JhI-1ΔMTS.T:SV5\V5 transgene as well as a Minute mutation (to give the JhI-1ED24 mutant clones a growth advantage) show a significant delay in the G[[2]]/M transition of the mitotic cell cycle compared to controls and a sharp increase in the production of reactive oxygen species (ROS) and DNA damage markers. However, no induction of apoptosis is observed in these clones either in the wing or the antenna imaginal discs. The JhI-1ED24;JhI-1ΔMTS.T:SV5\V5 wing disc cells have normal size.
RNaseZΔMTS.Tag:V5 partially rescues RNaseZED24
RNaseZhs.Tag:V5/RNaseZΔMTS.Tag:V5 partially rescues RNaseZED24
The survival of the JhI-1ED24 homozygous mutant larvae is prolonged by expression JhI-1ΔMTS.T:SV5\V5 in the mutant background, but the larval growth is arrested upon reaching the third instar stage and they die several weeks later as undersized third instar larvae.
JhI-1ED24 homozygous mutants expressing JhI-1ΔMTS.T:SV5\V5 arrest larval growth at third instar stage and develop only rudimentary imaginal discs. The growth of the wing and eye discs can be partially rescued by a single heat-shock induced pulse expression of JhI-1hs.T:SV5\V5 but the discs show significant increase in reactive oxygen species (ROS) production compared to controls.