Houchmandzadeh B, Wieschaus E, Leibler S
CNRS, Laboratoire Spectromtrie Physique, BP87, 38402 St-Martin d'Hres, France.
Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Dec;72(6 Pt 1):061920. doi: 10.1103/PhysRevE.72.061920. Epub 2005 Dec 30.
A simple morphogen gradient based on the protein bicoid is insufficient to explain the precise (i.e., similar in all embryos) setting of anteroposterior gene expression domains in the early Drosophila embryo. We present here an alternative model, based on quantitative data, which accounts for all of our observations. The model also explains the robustness of hunchback boundary setting in unnatural environments such as published recently [Luccheta, Nature 434, 1134 (2005)]. The model is based on the existence of a secondary gradient correlated to bicoid through protein degradation by the same agent.
基于蛋白质双尾的简单形态发生素梯度不足以解释果蝇早期胚胎中前后基因表达域精确的(即所有胚胎中相似的)设定。我们在此提出一种基于定量数据的替代模型,该模型解释了我们所有的观察结果。该模型还解释了在如最近发表的[卢切塔,《自然》434, 1134 (2005)]等非自然环境中驼背边界设定的稳健性。该模型基于存在一个与双尾相关的二级梯度,该二级梯度通过同一因子的蛋白质降解产生。