G18729522A
R397H | ChAT-PA; R397H | ChAT-PB
R397H
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
eye photoreceptor cell & axon & pupa | somatic clone | conditional ts
Synaptic currents recorded in Chats2 mutant second instar larvae raised at 18[o]C are significantly reduced.
Averaged synaptic current, recorded in aCC/RP2 neurons, in Chats2 larvae is significantly reduced compared to controls.
Eye photoreceptor axon projection is abberant in late third instar larvae (?) in which the developing retina contains large somatic clones of Chats2 homozygous cells and which have been raised at 30oC (a non-permissive temperature for this allele). Although the photoreceptor axons enter the optic stalk normally, they sometimes behave abnormally at the exit, and in rare cases form ectopic bundles that miss the lamina target field entirely. Mutant axons that enter the lamina establish an uneven distribution: growth cones fail to form a continuous plexus layer composed of R1-R6 axon termini. However, mistargeted axons do not extend into the medulla target field. Lamina neuronal differentiation and glial migration into the lamina target field is unaffected in these larvae, but these cells are not so precisely organised into distinct glial and neuronal layers as in wild-type. By late pupal stages, photoreceptor axons are segregated properly into lamina and medulla layers, but the projections are somewhat disorganized within each layer.
Mutant embryos raised at 29oC completely lack EPSCs and sustained currents in aCC/RP2. The arborisation of the aCC, including total area, maximum spread and position relative to the axon scaffold appears normal in these animals. The frequency of presynaptic endings adjacent to aCC remains unchanged compared to wild type. At 29oC, stimulation of the axons of aCC/RP2 continues to evoke excitatory junctional currents in the target muscles. At 18oC, the frequency of EPSCs and sustained currents is normal. aCC and RP2 have abnormal electrical properties in mutant embryos raised at 29oC. The peak current density of both total IKfast and INa is increased (these alterations are not seen in embryos raised at 18oC). When mutant embryos are shifted from 18 to 29oC at early stage 16 and maintained at 29oC for 5 hours (equivalent to 19 hours after egg laying at 25oC) they show an increase in the peak current density of IKfast in aCC/RP2 (recorded at a time equivalent to 20 hours after egg laying at 25oC). Embryos returned to 18oC after 5 hours at 29oC and allowed to develop show a delay in hatching, and show no significant increase in IKfast compared to age-matched controls (recorded at a time equivalent to 23 hours after egg laying at 25oC).
Chats2/Df(3R)Cha5 flies raised at 18oC and then transferred to 30oC can stand and walk around after 1 day at 30oC. The flies are all paralysed after 2 days at 30oC.
Monoclonal antibodies to CHA recognise a protein of wild-type molecular weight (80kD) but, even at the permissive temperature, in lesser amounts than in the wild-type.
ChATts2 has abnormal neurophysiology | heat sensitive phenotype, suppressible by DysRNAi.Dp186.UAS/Scer\GAL4eve.RN2
ChATts2 has abnormal neurophysiology | heat sensitive phenotype, non-suppressible by gbbUAS.cKa/Scer\GAL4eve.RN2
Overexpression of DysdsRNA.mub.Scer\UAS post-synaptically under the control of Scer\GAL4eve.RN2 suppresses the reduced synaptic currents found in Chats2 mutant second instar larvae raised at 18[o]C.
Overexpression of gbbScer\UAS.cKa post-synaptically under the control of Scer\GAL4eve.RN2 fails to suppress the reduced synaptic currents found in Chats2 mutant second instar larvae raised at 18[o]C.
Postsynaptic expression of gbbScer\UAS.cKa, under the control of Scer\GAL4eve.RN2, fails to potentiate synaptic current amplitude in aCC/RP2 neurons when expressed in a Chats2 homozygous background at 29oC, compared to in a Chats2/+ control background. If larvae are allowed to recover at 20oC for another 22 hours, the ability of gbbScer\UAS.cKa to potentiate synaptic current amplitude in a Chats2 background is restored.
The order for phenotypic severity for temperature-sensitive paralysis in adults is: Chats3 > Chats2 > Chats1.