The kinetics of cleavage furrow ingression during cellularisation are altered in mutant embryos compared to wild type. All three phases of ingression are faster than normal, with the final phase in particular being significantly faster than wild type.
Mutant larvae and adults are sluggish. Third instar larvae show about a 70% reduction in movement compared to controls. The number of boutons and amount of branching at the neuromuscular junction appear normal in mutant third instar larvae. The amplitude of miniature excitatory junctional currents at the neuromuscular junction in mutant third instar larvae is not significantly different from that of control larvae. Recovery from synaptic fatigue is not altered in mutant larvae compared to controls. There is no major difference in CNS-generated motor activity in mutant and control larvae.
AmphMI08903-TG4.0/Amph5E3 has abnormal locomotor behavior | adult stage phenotype, suppressible by Scer\GAL4Amph-MI08903-TG4.0/Hsap\BIN1UAS.8
Amph[+]/Amph5E3 is a suppressor of notal microchaeta phenotype of Hsap\MAPT4xA.UAS.2N4R, Scer\GAL4Eq
Amph[+]/Amph5E3 is a suppressor of eye phenotype of Hsap\MAPT4xA.UAS.2N4R, Scer\GAL4GMR.PF
Amph[+]/Amph5E3 is a suppressor of ommatidium phenotype of Hsap\MAPT4xA.UAS.2N4R, Scer\GAL4GMR.PF
A Amph5E3 heterozygous background suppresses Hsap\MAPT4xA.Scer\UAS.2N4R-induced toxicity, leading to a 30% increase in eye surface, compared with flies expressing solely Hsap\MAPT4xA.Scer\UAS.2N4R.
A Amph5E3 heterozygous background suppresses the Scer\GAL4Eq1>Hsap\MAPT4xA.Scer\UAS.2N4R-induced a bristle loss phenotype, resulting in 37% more notal bristles compared with flies expressing Scer\GAL4Eq1>Hsap\MAPT4xA.Scer\UAS.2N4R alone.
A Amph5E3 mutant background does not affect the subtle rough eye phenotype caused by expression of Hsap\APPAβ42.Scer\UAS.cUa under the control of Scer\GAL4elav-C155.