Ectopic expression of capsID.Scer\UAS, a construct lacking the intracellular part, in the developing eye, under the control of Scer\GAL4GMR.PF, display a mild R7 stopping phenotype.
Expression of capsID.Scer\UAS in both R7 and R8 photoreceptors, under the control of Scer\GAL4sev.PM181, generates a strong R7 axon stopping phenotype.
Expression of capsID.Scer\UAS in ventral muscle 12 causes synaptic terminal defects. In contrast, expression of capsID.Scer\UAS with Scer\GAL4elav.PLu in motoneurons does not lead to synaptic terminal abnormalities.
Embryos that express capsID.Scer\UAS under the control of Scer\GAL4twi.PG show normal development of the tracheal system.
Third instar larvae expressing capsID.Scer\UAS under the control of Scer\GAL4elav.PLu at 29oC show defects in the trajectory of the motorneurons that innervate muscle 12 in 19% of hemisegments. Expression of capsID.Scer\UAS under the control of Scer\GAL4how-24B does not result in an increased frequency of the terminals of motorneurons that normally innervate muscle 12 forming ectopic synapses on muscle 13.
capsID.UAS, Scer\GAL4ap-md544 is a suppressor of neoplasia | larval stage phenotype of EgfrUAS.cBa, Scer\GAL4ap-md544, psqKK111691
capsID.UAS, Scer\GAL4ap-md544 is a suppressor of increased cell number | larval stage phenotype of EgfrUAS.cBa, Scer\GAL4ap-md544, psqKK111691
capsID.UAS, Scer\GAL4ap-md544 is a suppressor of increased mortality during development phenotype of EgfrUAS.cBa, Scer\GAL4ap-md544, psqKK111691
capsID.UAS, Scer\GAL4ap-md544 is a suppressor of partially lethal phenotype of EgfrUAS.cBa, Scer\GAL4ap-md544, psqKK111691
Scer\GAL4twi.PG/capsID.UAS is an enhancer of tracheal dorsal trunk primordium phenotype of trn28.4
capsID.UAS, Scer\GAL4ap-md544 is a suppressor of wing disc phenotype of EgfrUAS.cBa, Scer\GAL4ap-md544, psqKK111691
All larvae co-expressing psqKK111691 and EgfrUAS.cBa under the control of Scer\GAL4ap-md544 during larval stages (using Gal80[ts] for the temporal regulation of expression) wing discs tumors, associated with higher numbers of myoblasts. These phenotypes are partially suppressed by the co-expression of capsID.UAS.
Expression of capsID.Scer\UAS under the control of Scer\GAL4twi.PG enhances the severity of the dorsal trunk defects of trn28.4 embryos.
capsID.Scer\UAS suppresses the loss of laterally located somatic clones of salmScer\UAS.cdCa; Scer\GAL4Act5C.PP cells in late third instar wing discs.