Fig. 3
- ID
- ZDB-FIG-230509-23
- Publication
- Nikolaou et al., 2022 - Cytoplasmic pool of U1 spliceosome protein SNRNP70 shapes the axonal transcriptome and regulates motor connectivity
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Figure 3. SNRNP70 is cell-autonomously required in motor neurons for neuromuscular assembly (A) A representative image showing transplanted sibling motor neurons derived from a Tg(mnx1:GFP) line innervating a WT host myotome that has been stained with anti-SV2 and α-BTX to mark pre- and post-synaptic sites, respectively. Bottom: inset depicting the apposition (red arrows) of pre- (within the GFP+ motor neurons) and post-synaptic sites within a small region of the myotome. Scale bars, 25 μm. (B and C) Examples of transplanted GFP+ null motor neurons innervating WT host myotomes that have been stained with anti-SV2 and α-BTX. In (B), null GFP+ motor axons terminate in a motor-axon-sparse region of the myotome, whereas in (C), they terminate in a motor-axon-dense region. Bottom: insets depicting the apposition (red arrows) of pre- (within the GFP+ motor neurons) and post-synaptic sites regions of the myotome. Cyan arrows indicate the absence of host AChR clusters adjacent to transplanted GFP+/SV2+ terminals. Scale bars, 25 μm. (D) Quantification of the degree of overlap between SV2 and α-BTX in the three groups of transplanted motor axons. The graph shows mean values ± SEM. ∗∗∗p< 0.001, one-way ANOVA, n = 6 donor/host pairs for sib-to-WT group, n = 3 donor/host pairs for null-to-WT group in three independent experiments. See also Figure S3. |