Institute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan.
Exp Biol Med (Maywood). 2010 Jul;235(7):796-804. doi: 10.1258/ebm.2010.009351. Epub 2010 Jun 11.
The family of WW domain-containing proteins contains over 2000 members. The small WW domain module is responsible, in part, for protein/protein binding interactions and signaling. Many of these proteins are located at the membrane/cytoskeleton area, where they act as adaptors to receive signals from the cell surface. In this review, we provide molecular insights regarding recent novel findings on signaling from the cell surface toward WW domain-containing oxidoreductase, known as WWOX, FOR or WOX1. More specifically, transforming growth factor beta 1 utilizes cell surface hyaluronidase Hyal-2 (hyaluronoglucosaminidase 2) as a cognate receptor for signaling with WWOX and Smad4 to control gene transcription, growth and death. Complement C1q alone, bypassing the activation of classical pathway, signals a novel event of apoptosis by inducing microvillus formation and WWOX activation. Deficiency in these signaling events appears to favorably support cancer growth.
WW 结构域蛋白家族包含超过 2000 个成员。WW 结构域模块的一小部分负责蛋白质/蛋白质结合相互作用和信号转导。许多这些蛋白质位于膜/细胞骨架区域,在那里它们充当接受来自细胞表面的信号的适配器。在这篇综述中,我们提供了关于 WW 结构域氧化还原酶(称为 WW0X、FOR 或 WOX1)的信号从细胞表面向 WW 结构域氧化还原酶传递的最新发现的分子见解。更具体地说,转化生长因子β 1 利用细胞表面透明质酸酶 Hyal-2(透明质酸葡糖胺糖苷酶 2)作为信号转导的同源受体,与 WW0X 和 Smad4 一起控制基因转录、生长和死亡。补体 C1q 单独绕过经典途径的激活,通过诱导微绒毛形成和 WW0X 激活来发出凋亡的新事件信号。这些信号事件的缺失似乎有利于支持癌症生长。