FlyBase curator comment: this entry represents a transgenic construct where the particular construct used cannot be determined.
Expression of commScer\UAS.cUa under the control of Scer\GAL415J2 causes contralateral misprojection of the dMP2 neuron along the anterior commissure of the next segment in 93.8% of cases. The pCC axon correctly follows the longitudinal pathway and contacts the dMP2 axon.
Scer\GAL4elav.PLu, commUAS.cUa, robo1ΔIg2-5.Tag:HA has abnormal neuroanatomy | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1ΔFn1-3.Tag:HA has abnormal neuroanatomy | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1ΔIg2ΔFn3.Tag:HA has abnormal neuroanatomy | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1Tag:HA has abnormal neuroanatomy | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1ΔIg2-5.Tag:HA has axon | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1Tag:HA has axon | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1ΔFn1-3.Tag:HA has axon | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1ΔIg2ΔFn3.Tag:HA has axon | embryonic stage phenotype
Scer\GAL4elav.PLu, commUAS.cUa, robo1Tag:HA has larval ventral nerve cord | embryonic stage phenotype
Co-expression of commScer\UAS.cUa (under the control of Scer\GAL4elav.PLu) and robo1T:Ivir\HA1 or robo1ΔIg1.T:Ivir\HA1 in embryos results in an increase in axon midline crossing and corresponding thickening of commissures in the ventral nerve cord.