Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis

被引:78
作者
Ribisi, S
Mariani, FV
Aamar, E
Lamb, TM
Frank, D
Harland, RM [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Technion Israel Inst Technol, Rappaport Med Sch, Dept Biochem, IL-31096 Haifa, Israel
基金
美国国家卫生研究院;
关键词
D O I
10.1006/dbio.2000.9889
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fibroblast growth factor (FGF) has been proposed to be involved in the specification and patterning of the developing vertebrate nervous system. There is conflicting evidence, however, concerning the requirement for FGF signaling in these processes. To provide insight into the signaling mechanisms that are important for neural induction and anterior-posterior neural patterning, we have employed the dominant negative Ras mutant, N17Ras, in addition to a truncated FGF receptor (XFD). Both N17Ras and XFD, when expressed in Xenopus laevis animal cap ectoderm, inhibit the ability of FGF to generate neural pattern. They also block induction of posterior neural tissue by XBF2 and XMeis3. However, neither XFD nor N17Ras inhibits noggin, neurogenin, or XBF2 induction of anterior neural markers. MAP kinase activation has been proposed to be necessary for neural induction, yet N17Ras inhibits the phosphorylation of MAP kinase that usually follows explantation of explants. In whole embryos, Pas-mediated FGF signaling is critical for the formation of posterior neural tissues but is dispensable for neural induction. (C) 2000 Academic Press.
引用
收藏
页码:183 / 196
页数:14
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