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XB-IMG-158942

Xenbase Image ID: 158942


Figure 10. Activin, but Not Noggin, Induces the Expression of Xenopus Follistatin (A) Animal cap exolants were isolated from btastulae (stage 8) and incubated in the presence or absence of activin. When sibling controls reached the gastrula stage (stage 10.5) total RNA was assayed by RT-PCR for XFS- expression. Explants incubated in the presence of activin induce the expression of follistatin. The embryo lane contains RNA from sibling controls (stage 10.5). The control lane contains all the ingredients of the embryo lane except for RT. The EF-1 o signal demonstrates that a comparable amount of RNA was assayed in each lane. (6) Left panel, 2-41 stage embryos were injected in the animal pole of both blastomeres with 1 ng of noggin RNAor control globin RNA. The explants were cut, harvested, cultured, and scored for XFS-319 RNA under the same conditions described for (A). Noggin does not induce the expression of follistatin RNA. Noggin in these experiments is active, since it was able directly to neuralize animal cap explants from the same experiment harvested at tailbud stage. (C) Activin induces the expression of follistatin in the context of the whole embryo. Embryos were injected at the &to 16-cell stage in a single vegetal blastomere with 2 pg of either Xenopus activin Bb or globin control RNA. Embryos were allowed to develop until early neurula stage (stage 21) and ware then assayed by whole-mount in situ hybridization for the expression of follistatin. While the control injected embryo at the right demonstrates a single primary axis (I), the embryo on the left injected with activin contains an ectopic axis (II) that stains positively for follistatin transcript. The in situ probe used in this study and the sense control probe (not shown) are the same as those in Figure 3.

Image published in: Hemmati-Brivanlou A et al. (1994)

Copyright © 1994. Image reproduced with permission of the Publisher, Elsevier B. V.

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