Department of Molecular and Medical Genetics, School of Medicine, Oregon Health & Science University, Portland, Oregon 97239, USA.
J Biol Chem. 2010 Aug 13;285(33):25812-21. doi: 10.1074/jbc.M109.098442. Epub 2010 Jun 16.
Ribosomal proteins play an important role in p53 activation in response to nucleolar stress. Multiple ribosomal proteins, including L5, L11, L23, and S7, have been shown to bind to and inhibit MDM2, leading to p53 activation. However, it is not clear whether ribosomal protein regulation of MDM2 is specific to some, but not all ribosomal proteins. Here we show that L29 and L30, two ribosomal proteins from the 60 S ribosomal subunit, do not bind to MDM2 and do not inhibit MDM2-mediated p53 suppression, indicating that the ribosomal protein regulation of the MDM2-p53 feedback loop is specific. Interestingly, direct perturbation of the 60 S ribosomal biogenesis by knocking down either L29 or L30 drastically induced the level and activity of p53, leading to p53-depedent cell cycle arrest. This p53 activation was drastically inhibited by knockdown of L11 or L5. Consistently, knockdown of L29 or L30 enhanced the interaction of MDM2 with L11 and L5 and markedly inhibited MDM2-mediated p53 ubiquitination, suggesting that direct perturbation of 60 S ribosomal biogenesis activates p53 via L11- and L5-mediated MDM2 suppression. Mechanistically, knockdown of L30 or L29 significantly increased the NEDDylation and nuclear retention of L11. Knocking down endogenous NEDD8 suppressed p53 activation induced by knockdown of L30. These results demonstrate that NEDDylation of L11 plays a critical role in mediating p53 activation in response to perturbation of ribosomal biogenesis.
核糖体蛋白在核仁应激反应中 p53 的激活中发挥重要作用。已经证实多种核糖体蛋白,包括 L5、L11、L23 和 S7,与 MDM2 结合并抑制其功能,从而导致 p53 的激活。然而,核糖体蛋白对 MDM2 的调节是否特异性针对某些核糖体蛋白,而不是所有核糖体蛋白,目前尚不清楚。在这里,我们发现 L29 和 L30,两个来自 60S 核糖体亚基的核糖体蛋白,不与 MDM2 结合,也不抑制 MDM2 介导的 p53 抑制,表明核糖体蛋白对 MDM2-p53 反馈回路的调节是特异性的。有趣的是,通过敲低 L29 或 L30 直接干扰 60S 核糖体的生物发生,大大诱导了 p53 的水平和活性,导致 p53 依赖性细胞周期停滞。这种 p53 的激活被 L11 或 L5 的敲低严重抑制。一致地,敲低 L29 或 L30 增强了 MDM2 与 L11 和 L5 的相互作用,并显著抑制了 MDM2 介导的 p53 泛素化,表明直接干扰 60S 核糖体的生物发生通过 L11 和 L5 介导的 MDM2 抑制激活 p53。在机制上,敲低 L30 或 L29 显著增加了 L11 的 NEDDylation 和核保留。敲低内源性 NEDD8 抑制了 L30 敲低诱导的 p53 激活。这些结果表明,L11 的 NEDDylation 在介导核糖体生物发生扰动时的 p53 激活中起着关键作用。