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. 2020 Jan 29;9:e50597. doi: 10.7554/eLife.50597

Figure 2. Innexins are required for mechanosensation and electrical coupling of touch neurons.

(A, B, C) Gentle touch responses recorded in ALM for wild type worms, worms in which AVM has been laser ablated and worms expressing dsRNA under control of Pmec-7. Neurons have been classified as ‘ipsilateral’ or ‘contralateral’, according to the position of the cell body relative to the stimulation site and the hypothetical midline of the animal. (A) Average traces of % ratio change. Gray indicates SEM. (B) Scatter plot showing individual ratio changes (diamonds). Bars indicate mean ± SEM. (C) Graph showing proportion exhibiting a Ca2+ response. Error bars indicate SE. In ipsilateral neurons, the proportion of AVM ablated animals (p=0.1686) or unc-9 RNAi animals (p=0.1686) responding is not significantly different to wild type, while unc-7 RNAi animals respond at a significantly reduced rate (p=0.0021). Combining unc-9 RNAi with AVM ablation is not significantly different from either unc-9 RNAi alone (p=0.7104), AVM ablation alone (p=0.6946) or unc-9(e101) (p=1). In contralateral neurons, the proportions of AVM ablated, unc-7 RNAi and unc-9 RNAi animals responding are all significantly lower than wild type (p=0.0012; p=0.0001; p=0.001). Combining unc-9 RNAi with AVM ablation is not significantly different from either unc-9 RNAi alone (p=1.0), AVM ablation alone (p=0.6027) or unc-9(e101) (p=0.661), Fisher’s exact test (N = 15, 14, 16, 16, 14, 24, 11, 8, 12, 14, 11, 22, in the order shown in C).

Figure 2.

Figure 2—figure supplement 1. unc-7 is required for gentle touch response in AVM.

Figure 2—figure supplement 1.

(A, B, C) Ca2+ response to 1 s buzz in AVM, for wild type and TRN-specific unc-7 RNAi animals. All AVM neurons assayed were located in the ‘near’ half of the animal, with respect to the stimulation site, as determined by the position of the cell body. (A) Average traces of % ratio change. Gray indicates SEM. (B) Scatter plot showing individual ratio changes (diamonds). Bars indicate mean ± SEM. (C) Graph showing proportion exhibiting a Ca2+ response. Error bars indicate SE. The proportion of AVM ‘near’ neurons responding is significantly lower in unc-7 RNAi animals compared to wild type (p=0.0128, Fisher’s exact test, N = 14, 13).
Figure 2—figure supplement 2. PLML and PLMR do not cooperate via gap junctions.

Figure 2—figure supplement 2.

(A, B, C) Ca2+ response to 1 s buzz in PLM, for wild type and TRN-specific unc-7 RNAi animals. (A) Average traces of % ratio change. Gray indicates SEM. (B) Scatter plot showing individual ratio changes (diamonds). Bars indicate mean ± SEM. (C) Graph showing proportion exhibiting a Ca2+ response. Error bars indicate SEM. The proportion responding is significantly lower in ‘contralateral’ neurons compared to those ipsilateral to the stimulation site (p<0.05, Fisher’s exact test, N = 14, 18, 16, 14, in the order shown in C).