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Fig. S2 Non-overlapping zic2aMOs cause similar patterning defects. (A, B) Embryos co-injected with translation-blocking MOs designed against the proximal promoter (zic2a P MO) and the first AUG (zic2a A MO) show similar arx reductions at 12s (4/20, 1 exp.) as embryos injected with splice-blocking zic2aMO (see Fig. 1). (C, D) Prim-5 stage embryos injected with zic2a A + P MO also show reduced dlx2a expression (14/45, 2 exp.) similar to zic2aMO-injected embryos (see Fig. 2).
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Reprinted from Developmental Biology, 317(1), Sanek, N.A., and Grinblat, Y., A novel role for zebrafish zic2a during forebrain development, 325-335, Copyright (2008) with permission from Elsevier. Full text @ Dev. Biol.