25.6kb deletion that removes the first 12 coding exons of Fife (deletion extends from 3L:2664461..2690083 ). A Disc\RFP3xP3.cUa marker has been inserted as part of the mutagenic event.
25.6 kb deletion removing the first 12 coding exons of Fife generated by CRISPR-mediated homology-directed repair.
The neurotransmission across neuromuscular junctions in third instar larvae, assessed by excitatory junction potential amplitude and quantal content, is significantly impaired in FifeAC homozygotes or FifeAC/Df(3L)Exel6091 transheterozygotes, but not in FifeAC heterozygotes, as compared to controls.
The neuromuscular junctions of FifeAC/Df(3L)Exel6091 transheterozygous third instar larvae present a significant decrease in the estimated mean readily releasable vesicle pool and an abnormal synaptic probability of release, as shown by their significantly higher facilitation in paired-pulse experiments, as compared to controls; these neuromuscular junctions also present defective active zones, as shown by a significant decrease in the mean number of membrane-associated synaptic vesicles in their vicinity, significant decreases in the width and complexity of their cytomatrix, and synaptic vesicles with similar numbers and similar mean distance from the membrane, but significantly less frequently docked to the membrane and significantly less frequently associated with the electron-dense cytomatrix, as compared to controls.
The neurotransmission across neuromuscular junctions of FifeAC/Fifeex1027 transheterozygous third instar larvae occurs with similar spontaneous miniature excitatory junction potentials, but decreased excitatory junction potentials and decreased quantal content, as compared to controls.
FifeAC, Rim[+]/Rim103 has abnormal neurophysiology | third instar larval stage phenotype
FifeAC, Rim[+]/Rim103 has embryonic/larval neuromuscular junction | third instar larval stage phenotype