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. 2017 Nov 9;8:1380. doi: 10.1038/s41467-017-01704-z

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Mutation of RYR-1 but not UNC-2 occluded synaptic and behavioral phenotypes of aipr-1(zw86). a, b Comparison of evoked currents a and spontaneous miniature currents (minis) b among wild type (wt) (n = 8), aipr-1(86) (n = 7), ryr-1(e540) (n = 7), aipr-1(zw86) ryr-1(e540) (n = 7), aipr-1(zw86) with muscle ryr-1 RNAi (n = 7), aipr-1(zw86) treated with ryanodine (100 µM) (n = 8), unc-2(e55) (n = 9), and aipr-1(zw86) unc-2(e55) (n = 7). c Comparison of thrashing rates among these groups (n = 12 or 13). Data are shown as mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001 compared with wt; ^# p < 0.05, ^## p < 0.01, ^### p < 0.001 compared between indicated groups; NS p > 0.05 (one-way ANOVA followed by Tukey’s post-hoc test)