Corey David P
Howard Hughes Medical Institute, Department of Neurobiology, Harvard Medical School 220 Longwood Avenue, Boston, MA 02115 USA.
F1000 Biol Rep. 2009 Jul 27;1:58. doi: 10.3410/B1-58.
The cloning of deafness genes, especially those for Usher syndrome, has helped to identify a variety of structural proteins involved in the development and function of hair-cell stereocilia. These include novel cadherins, a handful of myosin motors, and scaffolding proteins. Yet a new understanding of these proteins has upended the orthodox view of mechanosensation by hair cells.
耳聋基因的克隆,尤其是与Usher综合征相关的基因克隆,有助于识别参与毛细胞静纤毛发育和功能的多种结构蛋白。这些蛋白包括新型钙黏着蛋白、一些肌球蛋白马达蛋白和支架蛋白。然而,对这些蛋白质的新认识颠覆了毛细胞机械感受的传统观点。