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. Author manuscript; available in PMC: 2009 Jul 13.
Published in final edited form as: J Mol Cell Cardiol. 2007 May 18;43(3):243–253. doi: 10.1016/j.yjmcc.2007.05.008

Figure 4. Loss of zbmper causes a dorsalized phenotype.

Figure 4

(A) Western blot of zebrafish embryo lysates at 36hpf. Zbmper is effectively knocked down in embryos displaying the characteristic phenotype. (B–D) Lateral views of zebrafish embryos at different developmental stages. (B) Tail of a control zebrafish embryo at 48 hpf. (C) Tail of a representative zbmper morphant embryo at 36 hpf. The shape of the tail indicates a dorsalized phenotype. Somitic segments distal of the dorsal tail kick are smaller than in controls and are dysmorphic. Blood cells are pooled in the dorsal aorta proximal to the tail deformation (arrowhead). (D) Tail of a zbmper morphant embryo at 72 hpf. The tail has adopted a pigtail shape indicating a severely dorsalized phenotype.