Recombination between the Scer\FRT sites in the PBac{WH}Zaspf04847 and PBac{WH}Zaspf04784 insertions has resulted in a deletion that removes exons 5-9 and produces a frameshift.
lethal | embryonic stage (with Df(2R)Jp1)
12% of homozygotes die as embryos, while the majority of homozygotes die as first instar larvae. Most of the mutant larvae die within 24 hours of hatching. Those that survive longer never progress beyond the first larval instar (as shown by their small size and mouth hook morphology). Muscle contractions are slower in ZaspΔ larvae compared to wild type.
43% of ZaspΔ/Df(2R)Jp1 animals die as embryos, while the majority die as first instar larvae.
Late stage 17 ZaspΔ embryos lack the typical striated muscle pattern, indicating a Z line defect.
In freshly hatched ZaspΔ larvae, Z lines are either completely absent or are severely disorganised and irregularly spaced in ultrastructural analysis of the muscles. The filaments of the muscles are also disorganised and are no longer arranged in parallel arrays.
Muscle detachment defects are seen from stage 16 onwards in ZaspΔ embryos; the muscle fibers detach from myotendinous junctions. Some muscles are missing in some segments. Late stage 17 embryos occasionally show severe muscle detachment and rounding up of muscles. The muscle detachment is progressive (12% of embryos have rounded muscles at stage 17, but 98% of unhatched embryos have rounded muscles when analysed 24 hours later).
Zasp[+]/Zasp52Δ is an enhancer of presumptive embryonic/larval muscle system phenotype of ifSEF
Zasp52ZCL423 complements Zasp52Δ in lethal complementation and climbing tests.
"zaspΔ9" and "zaspΔ56" are independent isolates of an identical mutation, produced by recombination between the Scer\FRT sites in the PBac{WH}Zaspf04847 and PBac{WH}Zaspf04784 insertions.