Vargesson N, Kostakopoulou K, Drossopoulou G, Papageorgiou S, Tickle C
Department of Anatomy and Developmental Biology, University College London, London, United Kingdom.
Dev Dyn. 2001 Jan;220(1):87-90. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1083>3.0.CO;2-E.
We tested a diffusion gradient model for setting up overlapping domains of Hoxa gene expression in the chick limb bud. The model is based on morphogen production at the limb bud tip where the apical ridge is located and assumes that cells respond to a series of concentration thresholds. Consistent with the model, Hoxa13 gene expression rapidly switches off when the ridge is removed from stage 21/22 buds, while Hoxa11 and Hoxa10 expression is stable; Hoxa13 expression can be initiated and maintained in absence of the ridge by FGF soaked beads; the Hoxa13 domain first expands quickly and then slows up and the size is related to the dose of FGF4. Contrary to the model, addition of FGF4 to early limb buds does not activate Hoxa13 prematurely nor extend the Hoxa13 expression domain proximally. Therefore FGF4 signalling is necessary but not sufficient for Hoxa gene expression in the limb bud.
我们测试了一个扩散梯度模型,用于在鸡胚肢芽中建立Hoxa基因表达的重叠区域。该模型基于位于肢芽顶端(即顶端嵴所在位置)的形态发生素产生,并假设细胞对一系列浓度阈值做出反应。与该模型一致的是,当从21/22期芽中移除嵴时,Hoxa13基因表达迅速关闭,而Hoxa11和Hoxa10表达则保持稳定;通过FGF浸泡的珠子,在没有嵴的情况下可以启动并维持Hoxa13表达;Hoxa13区域首先快速扩展,然后速度减慢,其大小与FGF4的剂量有关。与该模型相反的是,向早期肢芽中添加FGF4不会过早激活Hoxa13,也不会向近端扩展Hoxa13表达区域。因此,FGF4信号对于肢芽中Hoxa基因表达是必要的,但不是充分的。