Chen Zhijian J, Sun Lijun J
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.
Mol Cell. 2009 Feb 13;33(3):275-86. doi: 10.1016/j.molcel.2009.01.014.
The small protein ubiquitin is a central regulator of a cell's life and death. Ubiquitin is best known for targeting protein destruction by the 26S proteasome. In the past few years, however, nonproteolytic functions of ubiquitin have been uncovered at a rapid pace. These functions include membrane trafficking, protein kinase activation, DNA repair, and chromatin dynamics. A common mechanism underlying these functions is that ubiquitin, or polyubiquitin chains, serves as a signal to recruit proteins harboring ubiquitin-binding domains, thereby bringing together ubiquitinated proteins and ubiquitin receptors to execute specific biological functions. Recent advances in understanding ubiquitination in protein kinase activation and DNA repair are discussed to illustrate the nonproteolytic functions of ubiquitin in cell signaling.
小蛋白泛素是细胞生死的核心调节因子。泛素最广为人知的作用是靶向26S蛋白酶体进行蛋白质降解。然而,在过去几年中,泛素的非蛋白水解功能被迅速发现。这些功能包括膜运输、蛋白激酶激活、DNA修复和染色质动力学。这些功能的一个共同机制是泛素或多聚泛素链作为一种信号,招募含有泛素结合结构域的蛋白质,从而将泛素化蛋白和泛素受体聚集在一起,执行特定的生物学功能。本文讨论了在蛋白激酶激活和DNA修复中理解泛素化的最新进展,以说明泛素在细胞信号传导中的非蛋白水解功能。