Soliman Mohamed A, Riabowol Karl
Department of Biochemistry University of Calgary, 3330 Hospital Drive N.W., Calgary, Alberta T2N 4N1, Canada.
Trends Biochem Sci. 2007 Nov;32(11):509-19. doi: 10.1016/j.tibs.2007.08.006. Epub 2007 Oct 18.
The INhibitor of Growth (ING) family of type II tumour suppressors are encoded by five genes in mammals (ING1-ING5), most of which encode multiple isoforms via splicing, and all of which contain a highly conserved plant homeodomain (PHD) finger motif. Since their discovery approximately ten years ago, significant progress has been made in understanding their subcellular targeting, their relationship to p53, their activation by bioactive phospholipids, and their key role in reading the histone code via PHD fingers, with subsequent effects on histone acetylation and transcriptional regulation. In the past year, we have begun to understand how ING proteins integrate stress signals with interpretation and modification of the histone epigenetic code to function as tumour suppressors.
II型肿瘤抑制因子生长抑制因子(ING)家族由哺乳动物中的五个基因(ING1 - ING5)编码,其中大多数基因通过剪接编码多种亚型,并且所有基因都包含一个高度保守的植物同源结构域(PHD)指基序。自大约十年前被发现以来,在理解它们的亚细胞定位、它们与p53的关系、它们被生物活性磷脂激活以及它们通过PHD指基序解读组蛋白密码从而对组蛋白乙酰化和转录调控产生后续影响等方面已经取得了重大进展。在过去的一年里,我们开始了解ING蛋白如何将应激信号与组蛋白表观遗传密码的解读和修饰整合起来,从而发挥肿瘤抑制因子的作用。