Yumimoto Kanae, Yamauchi Yuhei, Nakayama Keiichi I
Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Fukuoka 812-8582, Japan.
Cancers (Basel). 2020 May 15;12(5):1249. doi: 10.3390/cancers12051249.
Controlled protein degradation is essential for the operation of a variety of cellular processes including cell division, growth, and differentiation. Identification of the relations between ubiquitin ligases and their substrates is key to understanding the molecular basis of cancer development and to the discovery of novel targets for cancer therapeutics. F-box proteins function as the substrate recognition subunits of S-phase kinase-associated protein 1 (SKP1)-Cullin1 (CUL1)-F-box protein (SCF) ubiquitin ligase complexes. Here, we summarize the roles of specific F-box proteins that have been shown to function as tumor promoters or suppressors. We also highlight proto-oncoproteins that are targeted for ubiquitylation by multiple F-box proteins, and discuss how these F-box proteins are deployed to regulate their cognate substrates in various situations.
可控的蛋白质降解对于包括细胞分裂、生长和分化在内的多种细胞过程的运行至关重要。识别泛素连接酶与其底物之间的关系是理解癌症发展的分子基础以及发现癌症治疗新靶点的关键。F-box蛋白作为S期激酶相关蛋白1(SKP1)-Cullin1(CUL1)-F-box蛋白(SCF)泛素连接酶复合物的底物识别亚基发挥作用。在此,我们总结了已被证明具有肿瘤促进或抑制功能的特定F-box蛋白的作用。我们还强调了被多种F-box蛋白靶向泛素化的原癌蛋白,并讨论了这些F-box蛋白在各种情况下如何被部署以调节其同源底物。