UAS regulatory sequences drive expression of a mutant version of Hsap\L1CAM in which the cysteine at amino acid 264 has been replaced by tyrosine.
Expression of Hsap\L1CAMC264Y.Scer\UAS under the control of Scer\GAL4OK307 has no effect on Giant Fibre (GF) synapse functionality.
Hsap\L1CAMC264Y.UAS/Scer\GAL4shot-OK307 is a suppressor | partially of abnormal neurophysiology | adult stage phenotype of Nrg180ΔFIGQY, Nrgl4
Hsap\L1CAMC264Y.UAS/Scer\GAL4shot-OK307 is a suppressor | partially of abnormal neuroanatomy | adult stage phenotype of Nrg180ΔFIGQY, Nrgl4
Hsap\L1CAMC264Y.UAS/Scer\GAL4shot-OK307 is a non-suppressor of abnormal neuroanatomy | adult stage phenotype of Nrg849
Hsap\L1CAMC264Y.UAS/Scer\GAL4shot-OK307 is a suppressor | partially of giant fiber neuron | adult stage phenotype of Nrg180ΔFIGQY, Nrgl4
Hsap\L1CAMC264Y.UAS/Scer\GAL4shot-OK307 is a suppressor | partially of adult neuromuscular junction | adult stage phenotype of Nrg180ΔFIGQY, Nrgl4
Hsap\L1CAMC264Y.UAS/Scer\GAL4shot-OK307 is a non-suppressor of giant fiber neuron | adult stage phenotype of Nrg849
Expression of Hsap\L1CAMC264Y.Scer\UAS does not suppress the giant fibre axon guidance defects seen in Nrg849 mutant flies.
Expression of Hsap\L1CAMC264Y.Scer\UAS under the control of Scer\GAL4OK307 significantly suppresses the Giant Fibre (GF)-Trochanteral Muscle (TTM) synapse functional and morphological defects seen in flies expressing Nrg180ΔFIGQY in a Nrgl4 mutant background. Half of the tested GF to TTM connections are functionally normal, while the other half are functionally impaired.