Dai Mu-Shui, Sun Xiao-Xin, Lu Hua
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202, USA.
Mol Cell Biol. 2008 Jul;28(13):4365-76. doi: 10.1128/MCB.01662-07. Epub 2008 Apr 21.
The nucleolar protein nucleostemin (NS) is essential for cell proliferation and early embryogenesis. Both depletion and overexpression of NS reduce cell proliferation. However, the mechanisms underlying this regulation are still unclear. Here, we show that NS regulates p53 activity through the inhibition of MDM2. NS binds to the central acidic domain of MDM2 and inhibits MDM2-mediated p53 ubiquitylation and degradation. Consequently, ectopic overexpression of NS activates p53, induces G(1) cell cycle arrest, and inhibits cell proliferation. Interestingly, the knockdown of NS by small interfering RNA also activates p53 and induces G(1) arrest. These effects require the ribosomal proteins L5 and L11, since the depletion of NS enhanced their interactions with MDM2 and the knockdown of L5 or L11 abrogated the NS depletion-induced p53 activation and cell cycle arrest. These results suggest that a p53-dependent cell cycle checkpoint monitors changes of cellular NS levels via the impediment of MDM2 function.
核仁蛋白核干细胞因子(NS)对细胞增殖和早期胚胎发育至关重要。NS的缺失和过表达均会降低细胞增殖。然而,这种调节的潜在机制仍不清楚。在此,我们表明NS通过抑制MDM2来调节p53活性。NS与MDM2的中央酸性结构域结合,抑制MDM2介导的p53泛素化和降解。因此,NS的异位过表达激活p53,诱导G(1)期细胞周期停滞,并抑制细胞增殖。有趣的是,小干扰RNA敲低NS也会激活p53并诱导G(1)期停滞。这些效应需要核糖体蛋白L5和L11,因为NS的缺失增强了它们与MDM2的相互作用,而敲低L5或L11可消除NS缺失诱导的p53激活和细胞周期停滞。这些结果表明,一个p53依赖的细胞周期检查点通过阻碍MDM2功能来监测细胞NS水平的变化。