Extended Data Fig. 7: Morphological features of V2a IN subtypes.
From: Molecular blueprints for spinal circuit modules controlling locomotor speed in zebrafish

a, Esrrga+ V2a INs displayed only descending axonal projections. Arrow indicates continuing axonal projection. b, Lateral view of the morphology of two examples of Shox2+ V2a INs. c, vAChTa+ V2a INs mostly displayed bidirectional axonal projections. A specialized vAChTa+ V2a IN subtype showed located axonal projection and corresponds to the previously described escape V2a IN41. d, Box and whiskers plot of soma sizes of the three V2a INs subtypes (one-way ANOVA with Tukey’s post hoc multiple comparisons, ****p < 0.0001) (n = 12 Esrrga+; n = 12 Shox2+; n = 14 vAChTa+ V2a INs). e, Length of the axonal projections of Esrrga+ (magenta), Shox2+ (yellow) and vAChTa+ (blue) V2a INs (n = 5 neurons per subtype). f, V2a IN axons projected along topographically organized paths over the dorso-ventral and medio-lateral aspects of the spinal cord (n = 13 Esrrga+: magenta; n = 13 shox2+: yellow; n = 30 vAChTa+: blue). g, Recordings of a fast V2a IN displaying adapting firing that was recruited only at fast swimming frequency (>7-8 Hz). h, Top left: Example of dual patch-clamp recordings showing the lack of monosynaptic connection between a slow, Esrrga+ V2a IN and a fast MN. Bottom left: Morphological reconstruction of the recorded V2a IN-MN pair (black: soma and dendrites; red: V2a IN axons). Top right: Example of dual patch-clamp recording showing the absence of connections between a fast, vAChTa+ V2a IN and a slow MN. Bottom right: Morphological reconstruction of the recorded V2a IN-MN pair (black: soma and dendrites; red: V2a IN axons).