FGFR1 is independently required in both developing mid- and hindbrain for sustained response to isthmic signals

被引:148
作者
Trokovic, R
Trokovic, N
Hernesniemi, S
Pirvola, U
Weisenhorn, DMV
Rossant, J
McMahon, AP
Wurst, W
Partanen, J
机构
[1] Univ Helsinki, Viikki Bioctr, Inst Biotechnol, FIN-00014 Helsinki, Finland
[2] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[3] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[4] Tech Univ Munich, Inst Mammalian Genet, GSF, Res Ctr Environm & Hlth, D-85764 Neuhenberg, Germany
[5] Max Planck Inst Psychiat, D-80804 Munich, Germany
关键词
cerebellum; Cre recombinase; development; FGF; isthmic organizer; midbrain;
D O I
10.1093/emboj/cdg169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibroblast growth factors (FGFs) are signaling molecules of the isthmic organizer, which regulates development of the midbrain and cerebellum. Tissue-specific inactivation of one of the FGF receptor (FGFR) genes, Fgfr1, in the midbrain and rhombomere 1 of the hindbrain of mouse embryos results in deletion of the inferior colliculi in the posterior midbrain and vermis of the cerebellum. Analyses of both midbrain-hindbrain and midbrain-specific Fgfr1 mutants suggest that after establishment of the isthmic organizer, FGFR1 is needed for continued response to the isthmic signals, and that it has direct functions on both sides of the organizer. In addition, FGFR1 appears to modify cell adhesion properties critical for maintaining a coherent organizing center. This may be achieved by regulating expression of specific cell-adhesion molecules at the midbrain-hindbrain border.
引用
收藏
页码:1811 / 1823
页数:13
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