Department of Cellular and Molecular Medicine, University of California, San Diego, California 92093, USA.
Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a007864. doi: 10.1101/cshperspect.a007864.
Wnt proteins comprise a major family of signaling molecules that orchestrate and influence a myriad of cell biological and developmental processes. Although our understanding of the role of Wnt signaling in regulating development and affecting disease, such as cancer, has been ever increasing, the study of the Wnt proteins themselves has been painstaking and slow moving. Despite advances in the biochemical characterization of Wnt proteins, many mysteries remain unsolved. In contrast to other developmental signaling molecules, such as fibroblast growth factors (FGF), transforming growth factors (TGFβ), and Sonic hedgehog (Shh), Wnt proteins have not conformed to many standard methods of protein production, such as bacterial overexpression, and analysis, such as ligand-receptor binding assays. The reasons for their recalcitrant nature are likely a consequence of the complex set of posttranslational modifications involving several highly specialized and poorly characterized processing enzymes. With the recent description of the first Wnt protein structure, the time is ripe to uncover and possibly resolve many of the remaining issues surrounding Wnt proteins and their interactions. Here we describe the process of maturation of Wnt from its initial translation to its eventual release from a cell and interactions in the extracellular environment.
Wnt 蛋白构成了一类主要的信号分子家族,它们协调并影响着无数的细胞生物学和发育过程。尽管我们对 Wnt 信号在调节发育和影响疾病(如癌症)中的作用的理解一直在不断增加,但对 Wnt 蛋白本身的研究却一直很艰难且进展缓慢。尽管在 Wnt 蛋白的生化特性方面取得了进展,但仍有许多未解之谜。与其他发育信号分子(如成纤维细胞生长因子(FGF)、转化生长因子(TGFβ)和 Sonic hedgehog(Shh))不同,Wnt 蛋白不符合许多蛋白质生产的标准方法,例如细菌过表达和分析,例如配体-受体结合测定。它们顽固性质的原因可能是由于涉及几个高度专业化和特征描述较差的加工酶的一系列复杂的翻译后修饰。随着首个 Wnt 蛋白结构的描述,现在是时候揭示并可能解决围绕 Wnt 蛋白及其相互作用的许多剩余问题了。在这里,我们描述了 Wnt 从初始翻译到最终从细胞中释放并在细胞外环境中相互作用的成熟过程。