Deisenroth Chad, Zhang Yanping
Department of Radiation Oncology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Genes Cancer. 2011 Apr;2(4):392-403. doi: 10.1177/1947601911409737.
Cellular growth and division are two fundamental processes that are exquisitely sensitive and responsive to environmental fluctuations. One of the most energetically demanding functions of these processes is ribosome biogenesis, the key component to regulating overall protein synthesis and cell growth. Perturbations to ribosome biogenesis have been demonstrated to induce an acute stress response leading to p53 activation through the inhibition of Mdm2 by a number of ribosomal proteins. The energy status of a cell is a highly dynamic variable that naturally contributes to metabolic fluctuations, which can affect both the rates of ribosome biogenesis and p53 function. This, in turn, determines whether a cell is in an anabolic, growth-promoting state or a catabolic, growth-suppressing state. Here the authors integrate the known functions of p53 to postulate how changes in nutrient availability may induce the ribosomal protein-Mdm2-p53 signaling pathway to modulate p53-dependent metabolic regulation.
细胞生长和分裂是两个对环境波动极其敏感且能做出响应的基本过程。这些过程中能量需求最大的功能之一是核糖体生物合成,它是调节整体蛋白质合成和细胞生长的关键组成部分。已证明核糖体生物合成的扰动会通过多种核糖体蛋白抑制Mdm2从而诱导急性应激反应,导致p53激活。细胞的能量状态是一个高度动态的变量,自然会导致代谢波动,这会影响核糖体生物合成速率和p53功能。反过来,这决定了细胞处于合成代谢、促进生长的状态还是分解代谢、抑制生长的状态。在此,作者整合了p53的已知功能,以推测营养物质可用性的变化如何诱导核糖体蛋白-Mdm2-p53信号通路来调节p53依赖性代谢调控。