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. Author manuscript; available in PMC: 2011 Feb 26.
Published in final edited form as: Development. 2007 Feb 7;134(6):1061–1070. doi: 10.1242/dev.02805

Fig. 7. LvSnail functions downstream of LvAlx1 in PMCs.

Fig. 7

(A) Control embryos. (B) Embryos injected with AlxMASO show no PMC ingression. (C) Excess mesenchyme cells form in embryos overexpressing LvSnail. (D) Co-injection of LvSnail rescues the formation of mesenchyme cells in the absence of LvAlx1. (E) Diagram of experiment in F,G. vv, vegetal view. (F-F″) Chimeric embryos generated by combining one control micromere (green) and one AlxMASO-containing micromere (red) with a control 16-cell stage embryo in which two micromeres were removed. Brightfield (F), fluorescent (F′) and merged images (F″) show that the AlxMASO-containing micromere progeny do not ingress, unlike the control micromere progeny in the same embryos. (G-G″) LvSnail can rescue the effects of AlxMASO in PMC ingression. The micromere co-injected with Lvsnail mRNA and AlxMASO (green) ingresses into the blastocoele, whereas the AlxMASO-injected micromere (red) fails to ingress. Brightfield (G), fluorescent (G′), and merged (G″) images are shown.