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通过与结构相关的MDMX蛋白相互作用使MDM2癌蛋白稳定。

Stabilization of the MDM2 oncoprotein by interaction with the structurally related MDMX protein.

作者信息

Sharp D A, Kratowicz S A, Sank M J, George D L

机构信息

Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6069, USA.

出版信息

J Biol Chem. 1999 Dec 31;274(53):38189-96. doi: 10.1074/jbc.274.53.38189.

Abstract

The MDM2 oncoprotein has transforming potential that can be activated by overexpression, and it represents a critical regulator of the p53 tumor suppressor protein. To identify other factors with a potential role in influencing the expression and/or function of MDM2, we utilized a yeast two-hybrid screening protocol. Here we report that MDM2 physically interacts with a structurally related protein termed MDMX. The results obtained in these studies provide evidence that C-terminal RING finger domains, contained within both of these proteins, play an important role in mediating the association between MDM2 and MDMX. The interaction of these proteins interferes with MDM2 degradation, leading to an increase in the steady-state levels of MDM2. MDMX also inhibits MDM2-mediated p53 degradation, with subsequent accumulation of p53. Taken together, these data indicate that MDMX has the potential to regulate the expression and function of the MDM2 oncoprotein.

摘要

MDM2癌蛋白具有可通过过表达激活的转化潜能,并且它是p53肿瘤抑制蛋白的关键调节因子。为了鉴定在影响MDM2表达和/或功能方面具有潜在作用的其他因子,我们采用了酵母双杂交筛选方案。在此我们报告MDM2与一种称为MDMX的结构相关蛋白发生物理相互作用。这些研究中获得的结果提供了证据,表明这两种蛋白中所含的C末端环状结构域在介导MDM2与MDMX之间的关联中起重要作用。这些蛋白的相互作用干扰了MDM2的降解,导致MDM2稳态水平升高。MDMX还抑制MDM2介导的p53降解,随后导致p53积累。综上所述,这些数据表明MDMX具有调节MDM2癌蛋白表达和功能的潜力。

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