Bays Nathan W, Hampton Randolph Y
Exelixis, Inc., 170 Harbor Way, South San Francisco, California 94080, USA.
Curr Biol. 2002 May 14;12(10):R366-71. doi: 10.1016/s0960-9822(02)00862-x.
The ubiquitin-proteasome pathway has a well-defined beginning and end. Target proteins are initially recognized by upstream components and tagged with polyubiquitin chains. The 26S proteasome then degrades these polyubiquitinated proteins. Until recently, it was not known what, if any, steps occurred between the initial polyubiquitination of target proteins and their final degradation. Several new papers investigating the function of the Cdc48-Ufd1-Npl4 complex indicate that there is indeed a middle to the ubiquitin-proteasome pathway. The Cdc48-Ufd1-Npl4 complex functions in the recognition of several polyubiquitin-tagged proteins and facilitates their presentation to the 26S proteasome for processive degradation or even more specific processing. The elucidation of Cdc48, Ufd1 and Npl4 action not only provides long-sought functions for these specific proteins, but illuminates a poorly understood part of the ubiquitin-proteasome pathway.
泛素-蛋白酶体途径有明确的起始和结束。靶蛋白最初被上游组分识别并标记上多聚泛素链。然后26S蛋白酶体降解这些多聚泛素化的蛋白。直到最近,在靶蛋白最初的多聚泛素化与其最终降解之间发生了哪些步骤(如果有的话)尚不清楚。几篇研究Cdc48-Ufd1-Npl4复合物功能的新论文表明,泛素-蛋白酶体途径确实存在中间步骤。Cdc48-Ufd1-Npl4复合物在识别几种多聚泛素标记的蛋白中发挥作用,并促进它们呈递给26S蛋白酶体进行持续性降解或更特异性的加工。对Cdc48、Ufd1和Npl4作用的阐明不仅为这些特定蛋白提供了长期以来寻求的功能,还阐明了泛素-蛋白酶体途径中一个了解甚少的部分。