Haupt Susan, Louria-Hayon Igal, Haupt Ygal
Department of Pharmacy, The Hebrew University Hadassah Medical School, Jerusalem 91120, Israel.
J Cell Biochem. 2003 Jan 1;88(1):76-82. doi: 10.1002/jcb.10311.
The p53 protein is a key player in the cellular response to stress. Proper regulation of p53 is imperative for the suppression of tumor development. This regulation is largely governed by its master inhibitor, Mdm2, which both blocks p53 activities and promotes its destabilization. This tight regulation of p53 by Mdm2 must be interrupted under stress conditions in order for p53 to be stabilized in an active form. A combined action of partner proteins and modifying enzymes is essential for the relief of p53 from Mdm2. The recent revelation of p53 association with the PML-nuclear bodies provides one explanation of how this regulatory network is coordinated within the nucleus in response to certain stress conditions. Thus, it is not only the nature of the p53 regulatory complex but also the spatial and temporal context of this association that governs the output inhibitory signals mediated by p53.
p53蛋白是细胞应激反应中的关键因子。对p53的恰当调控对于抑制肿瘤发展至关重要。这种调控很大程度上由其主要抑制因子Mdm2控制,Mdm2既能阻断p53的活性,又能促进其不稳定。在应激条件下,Mdm2对p53的这种严格调控必须被打断,以便p53以活性形式稳定下来。伴侣蛋白和修饰酶的联合作用对于使p53从Mdm2中释放出来至关重要。最近发现p53与早幼粒细胞白血病蛋白核体相关,这为该调控网络如何在细胞核内响应特定应激条件进行协调提供了一种解释。因此,不仅p53调控复合物的性质,而且这种关联的时空背景都决定了由p53介导的输出抑制信号。