Expression of eyaE7.Scer\UAS under the control of Scer\GAL4dpp.blk1 does not cause ectopic eye development, abnormal leg development or a reduced eye phenotype.
eyaE7.UAS/Scer\GAL4dpp.blk1 is an enhancer of visible phenotype of Scer\GAL4dpp.blk1, dacUAS.cSa
Scer\GAL4dpp.blk1, eyaE7.UAS, soUAS.cPa has visible phenotype
Scer\GAL4dpp.blk1, dacUAS.cSa, eyaE7.UAS has eye | ectopic phenotype
Scer\GAL4dpp.blk1, eyaE7.UAS, soUAS.cPa has eye phenotype
Scer\GAL4dpp.blk1, eyaE7.UAS, soUAS.cPa has eye | ectopic phenotype
Scer\GAL4dpp.blk1, eyaE7.UAS, soUAS.cPa has leg phenotype
Scer\GAL4dpp.blk1, eyaE7.UAS, soUAS.cPa has antenna phenotype
Scer\GAL4dpp.blk1, eyaE7.UAS, soUAS.cPa has ommatidium | ectopic phenotype
eyaE7.Scer\UAS shows a synergy in ectopic eye formation when coexpressed under the control of Scer\GAL4dpp.blk1 with dacScer\UAS.cSa. Co-expression of eyaE7.Scer\UAS and soScer\UAS.cPa under the control of Scer\GAL4dpp.blk1 results in ectopic retinal tissue in 19% of cases. The ectopic retinal tissue consists of discernible ommatidia and is limited to the antennal region. Abnormal leg development is seen in 100% of cases, and in 12% of cases a reduced eye phenotype is seen.
Scer\GAL4ey.PB/eyaE7.UAS partially rescues eya2
The ability of eyaE7.Scer\UAS to rescue the eya2 mutant phenotype when expressed under the control of Scer\GAL4ey.PB is approximately one-fourth as strong as that of eyaScer\UAS.cBa (a wild-type transgene).