Fig. 1

Fig. 1 Disruption of NF–Y or TALE function affects anterior embryonic development. Zebrafish embryos were left uninjected (A, E, F, N, O) or injected with either control mRNA (GFP; B, G, H, P, Q), mRNA encoding a TALE dominant negative construct (PBCAB; C, I, J, R, S) or mRNA encoding an NF–Y dominant negative construct (NF-YA DN; D, K, L, T-W) at the 1–2 ​cell stage and raised to 24hpf (N–W), 28hpf (A–D) or 5dpf (E–L). Embryos were either left untreated (A–D), stained with alcian blue (E–L) or processed for detection of pax2 (at the mid/hindbrain boundary), krox20 (in rhombomeres 3 and 5) and hoxd4 (in the spinal cord) transcripts by in situ hybridization (N–W). White arrows highlight differences in eye morphology (A–L), black arrows highlight differences in head cartilage formation (E–L) and orange arrows indicate differences in rhombomere 3 krox20 expression (N–U). Tables summarize effects of TALE or NF–Y disruption on head cartilage formation (M), eye formation (X) and gene expression (Y). Panels V and W show representative images of embryos scored as having gross abnormalities in panel X. Embryos are shown in lateral (A-D, F, H, J, L, N, P, R, T, V) or dorsal (E, G, I, K, O, Q, S, U, W) views.