Mutants die at pupal stage P3.
Homozygous first and second instar larvae show normal morphology and locomotor/feeding behaviour. Third instar larvae show progressively less vigorous locomotion and feeding. Many mutants grow to normal size but remain in the food past the normal wandering stage and delay pupation for several days beyond the normal period. Neuromuscular morphology of mutants shows only minor alterations. Terminal branching pattern is similar to wild type, however mutants have 20% fewer terminal branches, due to fewer higher order branch segments at mutant terminals (assayed at muscle 12). This results in similarly reduced numbers of boutons on muscle 12 and 6/7, but not muscle 4. Mutant EJC amplitudes (muscle 12 and muscle 6) are significantly larger than wild type at all Ca2+ concentrations. mEJCs display no significant differences in mean amplitude, variability, spontaneous frequency or current decay kinetics compared to wild type. Short term synaptic facilitation, synaptic augmentation and posttetanic potentiation are strongly impaired in mutants. Synaptic plasticity defects are incompletely restored by reducing basal transmitter release.
Decrement in 15-minute memory retention.
Orc3lE49 is rescued by Orc3+t17.1
Complementation statement based on recessive pupal lethality phenotype.