Ponnuswamy A, Fahraeus R
Regional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Klin Onkol. 2012;25 Suppl 2:2S32-7.
The regulation of p53 expression levels is critical in controlling p53 activity in normal and damaged cells. This is well illustrated by the E3 ubiquitin ligase MDM2 that targets p53 for proteasomal degradation under normal conditions and is essential for controlling p53 activity during development. MDM2 is over-expressed in human cancers and together with some other E3 ligases that have also been implicated in controlling p53 stability, which emphasises the importance of post-translational regulation of p53 expression. At the level of synthesis, TP53 mRNA levels do not change in response to stresses and it is instead its rate of translation initiation that provides the mechanism of choice for expression control. More recent work has shown that TP53 mRNA plays an important role in mediating the cellular regulation of p53 activity. We will discuss the regulation of p53 synthesis and its implications for controlling p53 activity under normal conditions and during different types of stress response.
在正常细胞和受损细胞中,p53表达水平的调控对于控制p53活性至关重要。E3泛素连接酶MDM2很好地说明了这一点,在正常条件下,MDM2靶向p53进行蛋白酶体降解,并且在发育过程中对于控制p53活性至关重要。MDM2在人类癌症中过度表达,并且与其他一些也参与控制p53稳定性的E3连接酶一起,这强调了p53表达的翻译后调控的重要性。在合成水平上,TP53 mRNA水平不会因应激而改变,相反,其翻译起始速率为表达控制提供了选择机制。最近的研究表明,TP53 mRNA在介导p53活性的细胞调控中起重要作用。我们将讨论p53合成的调控及其在正常条件下和不同类型应激反应期间控制p53活性的意义。