FGF signaling controls somite boundary position and regulates segmentation clock control of spatiotemporal Hox gene activation

被引:532
作者
Dubrulle, J [1 ]
McGrew, MJ [1 ]
Pourquié, O [1 ]
机构
[1] Univ Mediterranee AP Marseille, Dev Biol Inst Marseille, Lab Genet & Physiol Dev, CNRS,INSERM, F-13288 Marseille 09, France
基金
澳大利亚研究理事会;
关键词
D O I
10.1016/S0092-8674(01)00437-8
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
Vertebrate segmentation requires a molecular oscillator, the segmentation clock, acting in presomitic mesoderm (PSM) cells to set the pace at which segmental boundaries are laid down. However, the signals that position each boundary remain unclear. Here, we report that FGF8 which is expressed in the posterior PSM, generates a moving wavefront at which level both segment boundary position and axial identity become determined. Furthermore, by manipulating boundary position in the chick embryo, we show that Hox gene expression is maintained in the appropriately numbered somite rather than at an absolute axial position. These results implicate FGF8 in ensuring tight coordination of the segmentation process and spatiotemporal Hox gene activation.
引用
收藏
页码:219 / 232
页数:14
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