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Fig. 3. Interfering with XSRF function changes cell fates. (A,B)
Phenotypes of embryos injected with DN XSRF RNA dorsally as compared with
uninjected embryos. (C,D) Embryos were injected at the four-cell stage
in the animal pole region with DN XSRF mRNA (1-2 ng) and the animal cap
explants cut at stage 8.5 were cultured to stage 10.25 in the presence or
absence of Activin protein (5 ng/ml) and then analyzed by RT-PCR. (C) DN XSRF
alone induced mesoderm (Chordin and VegT), endoderm (Sox17ß) and neural
(Zic3) markers in animal caps. Epidermal keratin (Exkeratin), an
epidermal marker, was reduced by injection of DN XSRF. (D) DN XSRF enhanced
the ability of Activin to induce target genes in animal caps. ODC was used as
a loading control; Uninjected, uninjected control animal caps.