LaBonne C, Whitman M
Program in Cell and Developmental Biology, Harvard Medical School, Boston, MA 02115.
Development. 1994 Feb;120(2):463-72. doi: 10.1242/dev.120.2.463.
We have examined the role of FGF signaling during activin-mediated mesoderm induction in Xenopus. Using dominant inhibitory mutants of FGF signal transducers to disrupt the FGF-signaling pathway at the plasma membrane or in the cytosol prevents animal cap blastomeres from expressing several mesodermal markers in response to exogenous activin. Dominant inhibitory mutants of the FGF receptor, c-ras or c-raf inhibit the ability of activin to induce molecular markers of both dorsal and ventral mesoderm including Xbra, Mix1 and Xnot. Some transcriptional responses to activin such as goosecoid and Xwnt8 are inhibited less effectively than others, however, suggesting that there may differing requirements for an FGF signal in the responses of mesoderm-specific genes to activin induction. Despite the requirement for this signaling pathway during activin induction, downstream components of this pathway are not activated in response to activin, suggesting that activin does not signal directly through this pathway.
我们研究了成纤维细胞生长因子(FGF)信号在非洲爪蟾中激活素介导的中胚层诱导过程中的作用。使用FGF信号转导子的显性抑制突变体在质膜或胞质溶胶中破坏FGF信号通路,可阻止动物帽卵裂球响应外源性激活素而表达几种中胚层标记物。FGF受体、c-ras或c-raf的显性抑制突变体抑制激活素诱导背侧和腹侧中胚层分子标记物的能力,这些标记物包括Xbra、Mix1和Xnot。然而,对激活素的一些转录反应,如 goosecoid和Xwnt8,受到的抑制比其他反应要小,这表明中胚层特异性基因对激活素诱导的反应中,对FGF信号可能有不同的需求。尽管在激活素诱导过程中需要这条信号通路,但该通路的下游成分并不会因激活素而被激活,这表明激活素不会直接通过这条通路发出信号。