Estimated endpoints of a deletion resulting from FLP-catalyzed recombination using the FRT-containing transposons PBac{RB}e00269 and P{XP}d07098.
Recombination between the two progenitor insertions has resulted in a deletion that removes the entire tal transcription unit.
talpri-1/talpri-2 embryos show a number of cuticle phenotypes; they completely lack denticle belts and dorsal hairs, and the head skeleton and posterior spiracles are deformed. The mutant embryos lack the specific F-actin accumulation that is normally seen at the site of denticle formation, but the F-actin signal at the cell boundaries remains in the presumptive denticle cells.
talpri-1/talpri-3 embryos show defects in the dorsal branches and transverse connectives of the tracheal system, including a loss of tracheal network integrity and an irregular tube diameter. The dorsal trunk lacks characteristic F-actin structures in the mutant embryos compared to wild type and the F-actin is disorganised
talpri-1/talpri-2 embryos lack the taenidial folds in the tracheal system.
talpri-2/talpri-1 is rescued by Scer\GAL4arm.PS/talORF1.UAS
talpri-2/talpri-1 is rescued by talORF3.UAS/Scer\GAL4arm.PS
talpri-2/talpri-1 is rescued by talORF4.UAS/Scer\GAL4arm.PS
talpri-2/talpri-1 is not rescued by Scer\GAL4arm.PS/tal1-4FS.UAS