Fig. 5 Protein product localization in mutant retinae. At 24 hpf, N-cadherin polypeptide is present in wild-type (A), glom117 (B) but not in pactm101b (C) retinae. This situation persists at later stages of development as shown for the wild-type (D), glom117 mutants (E), and pactm101b mutants (F). Residual staining present in (C) and (F) is most likely due to background fluorescence. As reported previously in wild-type animals, N-cadherin is expressed in plexiform layers (arrows in D and G) and in the optic nerve (arrowheads D in G). The glom117 mutant polypeptide appears to retain this distribution. It is present both in the optic nerve (arrowheads in E and H) and in ectopically localized plexiform patches (arrows in E and H). Western blotting indicates that N-cadherin polypeptide is absent in pactm101b/tm101b mutant embryos (I) but it persists in glom117/m117 animals (J) at 3 dpf. (D, E, G, H) Retinae at 50 hpf. Retina in (F) is at 72 hpf. “le” indicates lens. Arrowheads in (A–C) indicate the midline. In (A–H) dorsal is up.
Reprinted from Developmental Biology, 259(1), Malicki, J., Jo, H., and Pujic, Z., Zebrafish N-cadherin, encoded by the glass onion locus, plays an essential role in retinal patterning, 95-108, Copyright (2003) with permission from Elsevier. Full text @ Dev. Biol.