Expression of robo1T:Ivir\HA1 in the wild-type background has no discernible effect on the structure and morphology of the embryonic ventral nerve cord, not even when two copies of the transgene are present.
Expression of one or two copies of robo1T:Ivir\HA1 in embryos does not produce any obvious phenotypes in the ventral nerve cord.
Scer\GAL4elav.PLu, commUAS.Tag:HA, robo1Tag:HA has abnormal neuroanatomy | embryonic stage phenotype
commΔe39, robo11, robo1Tag:HA has abnormal neuroanatomy | embryonic stage phenotype
Scer\GAL4elav.PLu, robo11, robo1Tag:HA, robo2UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy | embryonic stage phenotype
commΔe39, robo11, robo1Tag:HA has commissure | embryonic stage phenotype
commΔe39, robo11, robo1Tag:HA has embryonic midline of ventral nerve cord phenotype
Scer\GAL4elav.PLu, robo11, robo1Tag:HA, robo2UAS.Tag:HA,Tag:SS(wg) has axon | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1Tag:HA has axon | embryonic stage phenotype
Co-expression of commScer\UAS.cUa (under the control of Scer\GAL4elav.PLu) and robo1T:Ivir\HA1 in embryos results in an increase in axon midline crossing and corresponding thickening of commissures in the ventral nerve cord.
robo1Tag:HA rescues robo11
robo1Tag:HA rescues robo11
robo1Tag:HA rescues robo11
robo1Tag:HA rescues robo11
robo1Tag:HA rescues robo11
Expression of robo1T:Ivir\HA1 in robo11 mutant background fully rescues the defects in midline repulsion characteristic for robo11 mutants and restores the normal appearance of the axon scaffold in the embryonic ventral nerve cord.
Expression of two copies of robo1T:Ivir\HA1 rescues the ventral nerve cord defects, FasII-expressing axon guidance defects and pCC guidance defects of robo11/robo11 mutant embryos.