Borsani G, DeGrandi A, Ballabio A, Bulfone A, Bernard L, Banfi S, Gattuso C, Mariani M, Dixon M, Donnai D, Metcalfe K, Winter R, Robertson M, Axton R, Brown A, van Heyningen V, Hanson I
Telethon Institute of Genetics and Medicine, Universitá Vita e Salute San Raffaele and Department of Biological Technological Research (DIBIT), San Raffaele Biomedical Science Park, Milan, Italy.
Hum Mol Genet. 1999 Jan;8(1):11-23. doi: 10.1093/hmg/8.1.11.
We have isolated a family of four vertebrate genes homologous to eyes absent (eya), a key regulator of ocular development in Drosophila. Here we present the detailed characterization of the EYA4 gene in human and mouse. EYA4 encodes a 640 amino acid protein containing a highly conserved C-terminal domain of 271 amino acids which in Drosophila eya is known to mediate developmentally important protein-protein interactions. Human EYA4 maps to 6q23 and mouse Eya4 maps to the predicted homology region near the centromere of chromosome 10. In the developing mouse embryo, Eya4 is expressed primarily in the craniofacial mesenchyme, the dermamyotome and the limb. On the basis of map position and expression pattern, EYA4 is a candidate for oculo-dento-digital (ODD) syndrome, but no EYA4 mutations were found in a panel of ODD patients.
我们已经分离出了一个由四个脊椎动物基因组成的家族,它们与果蝇眼睛发育的关键调节因子“无眼”(eya)同源。在此,我们展示了人类和小鼠中EYA4基因的详细特征。EYA4编码一种640个氨基酸的蛋白质,该蛋白质包含一个由271个氨基酸组成的高度保守的C末端结构域,在果蝇eya中,已知该结构域介导具有重要发育意义的蛋白质-蛋白质相互作用。人类EYA4定位于6q23,小鼠Eya4定位于10号染色体着丝粒附近的预测同源区域。在发育中的小鼠胚胎中,Eya4主要在颅面间充质、皮肌节和肢体中表达。基于图谱位置和表达模式,EYA4是眼-牙-指(ODD)综合征的一个候选基因,但在一组ODD患者中未发现EYA4突变。