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. 2014 Jun 14;3:e02224. doi: 10.7554/eLife.02224

Figure 3. Pou3f1 promotes neural fate commitment in vivo.

(A) Whole-mount in situ hybridization of Pou3f1 in early mouse embryos (E5.5–E8.0). The arrowhead marks the position-plane of the transverse section of the corresponding embryo below. Scale bars, 100 μm. (B) Contribution of injected GFP-labeled control (Ctrl), Pou3f1-knockdown (Pou3f1-KD), and inducible Pou3f1-overexpressing (Pou3f1-OE) ESCs to different germ lineages in chimeric embryos. NE, neuroectoderm; M, mesenchyme; and S, somite. Scale bars, 50 μm. (C) Statistical analysis of GFP-positive cell distribution in the various germ layer lineages in the ESC blastocyst injection study. The values represent the mean ± SD for C.

DOI: http://dx.doi.org/10.7554/eLife.02224.009

Figure 3.

Figure 3—figure supplement 1. Information of chimeric mice generated from Pou3f1-overexpressing or knockdown ESCs.

Figure 3—figure supplement 1.