Fig. S6

Zebrafish fu Takes Part in the Degradation of BMP Receptors and the Regulation of Dorsal-Ventral Patterning, Related to Figure 7

(A–F) fu mRNA is maternally and ubiquitously distributed in the early stages of zebrafish embryos, as detected by whole-mount in situ hybridization (A–E) and RT-PCR (F) from the one-cell stage to 24 hpf. All the embryos were of the lateral views, with dorsal to the right, at the shield stage. (G–J) fu mRNA overexpression downregulates zalk3-GFP expression in vivo.

(G and I) 200 pg zalk3-GFP mRNA was injected alone into one-cell stage embryos. GFP expression was observed and photographed at the 60% epiboly and 3-somite stages, respectively.

(H and J) 300 pg fu mRNA was co-injected with 200 pg zalk3-GFP mRNA at the one-cell stage. Compared with injection of zalk3-GFP mRNA alone, GFP expression in the embryos co-injected with fu mRNA became obviously weaker. (K–Y) fu mRNA overexpression inhibits dorsalization caused by BMP signaling downregulation.

(K–V) The genetic relationship between Fu and BMP signals in dorsal-ventral patterning. Overexpression of tBr mRNA (300 pg), which encodes a well-defined dominant negative form of the BMP type I receptor (Graff et al., 1994), caused gsc expansion in the organizer (L) and gata2 suppression in the ventral ectoderm (P) at the shield stage and gata1 suppression in the intermediate cell mass at 22 hpf (T), all of which were partially rescued by co-injection of 300 pg fu mRNA (M, Q, U). Co-injection with 5 ng fu-MO and p53MO did not show any rescue effects compared with tBr mRNA injection alone (N, R, V).

(W–Y) Statistical data for (K–V) are shown.