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Fig. 1

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ZDB-IMAGE-170620-4
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Figures for Miller et al., 2017
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Fig. 1

gjd1a/cx34.1 is required for electrical synapse formation.

(A) Schematic of an electrical synapse, a specialized neuronal gap junction. (B) Simplified schematic of the zebrafish Mauthner (M) circuit in dorsal view with anterior to the left. Neurons and synapses of the hindbrain and two, of 30, spinal segments are shown. In the hindbrain mixed electrical/chemical synapses are made between auditory (Aud) afferent neurons and the M cell lateral dendrite (Aud/M electrical synapses). In the spinal cord the M axon makes electrical synapses with commissural local (CoLo) interneurons found in each segment (M/CoLo electrical synapses). (C,D) Two representative dorsal views of spinal cord segments from M/CoLo:GFP larvae at 5 days post fertilization. Images are maximum intensity projections of ~10 uM with anterior to the left. Scale bar = 10 uM. Larvae are stained for anti-GFP (magenta), anti-human-Connexin36 (Cx36, yellow), and for neurofilaments (RMO44, blue). Individual GFP and Cx36 channels are shown in neighboring panels. Associated experimental statistics are found in the figure-related table. The Cx36 staining found at wildtype M/CoLo synapses (C), red circles) is lost in dis3 mutants (D), red circles). (E) Genome wide RNA-seq-based mapping data. The average frequency of mutant markers (black marks) is plotted against genomic position. A single region on chromosome 5 (chr5) emerges with an allele frequency near 1.0 indicating linkage to the dis3 mutation (red arrow). Each chromosome is separated by vertical lines and labeled at the bottom. (F) Mutant reads from the RNA-seq mapping data at two separate positions within the gjd1a/cx34.1 gene are shown aligned to the reference genome identifying two missense changes within dis3 mutant animals. Wildtype reference (ref) genome nucleotides and encoded amino acids (aa) are noted. Aligned mutant (MUT) reads are shown as grey boxes; colored letters highlights differences from reference. (G) Electrical synapses are lost in trans-heterozygous animals carrying a dis3 and an 8 bp frameshift allele (dis3/8 bp) in gjd1a/cx34.1. Images of the spinal cord as in (C,D). Associated quantitation of Cx36 at wildtype or mutant synapses can be found in source data for Figure 1.

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