Nery Flávia C, Rui Edmilson, Kuniyoshi Taís M, Kobarg Jörg
Centro de Biologia Molecular Estrutural, Laboratório Nacional de Luz Síncrotron, Rua Giuseppe Máximo Scolfaro 10.000, C.P. 6192, 13084-971 Campinas, SP, Brazil.
Biochem Biophys Res Commun. 2006 Mar 17;341(3):847-55. doi: 10.1016/j.bbrc.2006.01.036. Epub 2006 Jan 23.
Ki-1/57 is a cytoplasmic and nuclear phospho-protein of 57 kDa and interacts with the adaptor protein RACK1, the transcription factor MEF2C, and the chromatin remodeling factor CHD3, suggesting that it might be involved in the regulation of transcription. Here, we describe yeast two-hybrid studies that identified a total of 11 proteins interacting with Ki-1/57, all of which interact or are functionally associated with p53 or other members of the p53 family of proteins. We further found that Ki-1/57 is able to interact with p53 itself in the yeast two-hybrid system when the interaction was tested directly. This interaction could be confirmed by pull down assays with purified proteins in vitro and by reciprocal co-immunoprecipitation assays from the human Hodgkin analogous lymphoma cell line L540. Furthermore, we found that the phosphorylation of p53 by PKC abolishes its interaction with Ki-1/57 in vitro.
Ki-1/57是一种分子量为57 kDa的细胞质和细胞核磷酸化蛋白,它与衔接蛋白RACK1、转录因子MEF2C以及染色质重塑因子CHD3相互作用,这表明它可能参与转录调控。在此,我们描述了酵母双杂交研究,该研究共鉴定出11种与Ki-1/57相互作用的蛋白,所有这些蛋白都与p53或p53蛋白家族的其他成员相互作用或在功能上相关。当直接测试相互作用时,我们进一步发现Ki-1/57能够在酵母双杂交系统中与p53本身相互作用。这种相互作用可以通过体外纯化蛋白的下拉实验以及来自人霍奇金淋巴瘤类似细胞系L540的相互免疫共沉淀实验得到证实。此外,我们发现蛋白激酶C(PKC)介导的p53磷酸化在体外消除了它与Ki-1/57的相互作用。