Fig. S4
- ID
- ZDB-FIG-170220-18
- Publication
- Linsley et al., 2017 - Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3
- Other Figures
- All Figure Page
- Back to All Figure Page
DHPR particles and tetrads are reduced in stac3 mutants but Ryr feet are unaffected. (A) Transverse EM section showing the RyR feet (arrows) at triads in a WT muscle fiber (96 hpf). (B and C) Examples of transverse EM sections showing that the distribution of RyR feet (arrows) in stac3−/− muscles is comparable to that in WT muscles. (D) Histogram showing that the spacing of tetrads was comparable in fibers from WT (n = 39) and stac3−/− (n = 25). stac3−/− expressing Stac3WT (WT rescue, n = 45) and stac3−/− expressing Stac3NAM (NAM rescue, n = 44) larvae (ANOVA, P = 0.07). (E) Histogram showing that the spacing of RyR feet was comparable in WT (n = 27) and stac3−/− (n = 39) fibers (t test, P = 0.11). SEMs are indicated. |