Department of Molecular Biology, Institute of Basic Medical Science, PLA General Hospital, Beijing, China.
Ageing Res Rev. 2013 Jan;12(1):276-81. doi: 10.1016/j.arr.2012.07.002. Epub 2012 Jul 31.
The PH domain-containing casein kinase 2 interacting protein-1 (CKIP-1, also known as PLEKHO1) acts as a scaffold protein mediating interactions with multiple proteins, including CK2α, CPα, AP-1/c-Jun, Akt, ATM, IFP35/Nmi and Smurf1. CKIP-1 functions through different ways, such as plasma membrane recruitment, transcriptional activity modulation and posttranscriptional modification regulation. Moreover, the subcellular localization of CKIP-1 is determined by several key amino acids in a cell type dependent style, and the nucleus/plasma membrane shuttle of CKIP-1 is regulated by different cell stresses. As an adaptor protein, CKIP-1 is involved in various important signaling pathways, controlling cell growth, apoptosis, differentiation, cytoskeleton and bone formation. Strikingly, CKIP-1 has been recently demonstrated to be a promising target for treatment of osteoporosis in rat models. In addition, more evidences suggest that CKIP-1 might also function as a potential tumor suppressor.
PH 结构域包含的酪蛋白激酶 2 相互作用蛋白-1(CKIP-1,也称为 PLEKHO1)作为一种支架蛋白,介导与多种蛋白质的相互作用,包括 CK2α、CPα、AP-1/c-Jun、Akt、ATM、IFP35/Nmi 和 Smurf1。CKIP-1 通过多种方式发挥作用,如质膜募集、转录活性调节和转录后修饰调节。此外,CKIP-1 的亚细胞定位取决于不同细胞类型中的几个关键氨基酸,并且 CKIP-1 的核/质膜穿梭由不同的细胞应激调节。作为一种衔接蛋白,CKIP-1 参与了各种重要的信号通路,控制细胞生长、凋亡、分化、细胞骨架和骨形成。值得注意的是,CKIP-1 最近被证明是治疗骨质疏松症的大鼠模型中一个很有前途的靶点。此外,越来越多的证据表明,CKIP-1 也可能作为一种潜在的肿瘤抑制因子发挥作用。