作者
Kogo Takamiya, Vassiliki Kostourou, Susanne Adams, Shalini Jadeja, Georges Chalepakis, Peter J Scambler, Richard L Huganir, Ralf H Adams
发表日期
2004/2/1
期刊
Nature genetics
卷号
36
期号
2
页码范围
172-177
出版商
Nature Publishing Group US
简介
Cell adhesion to extracellular matrix (ECM) proteins is crucial for the structural integrity of tissues and epithelial-mesenchymal interactions mediating organ morphogenesis,. Here we describe how the loss of a cytoplasmic multi-PDZ scaffolding protein, glutamate receptor interacting protein 1 (GRIP1), leads to the formation of subepidermal hemorrhagic blisters, renal agenesis, syndactyly or polydactyly and permanent fusion of eyelids (cryptophthalmos). Similar malformations are characteristic of individuals with Fraser syndrome and animal models of this human genetic disorder, such as mice carrying the blebbed mutation (bl) in the gene encoding the Fras1 ECM protein,. GRIP1 can physically interact with Fras1 and is required for the localization of Fras1 to the basal side of cells. In one animal model of Fraser syndrome, the eye-blebs (eb) mouse, Grip1 is disrupted by a deletion of two coding exons. Our data …
引用总数
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