Shvarts A, Steegenga W T, Riteco N, van Laar T, Dekker P, Bazuine M, van Ham R C, van der Houven van Oordt W, Hateboer G, van der Eb A J, Jochemsen A G
Laboratory of Molecular Carcinogenesis, Sylvius Laboratories, Leiden University, The Netherlands.
EMBO J. 1996 Oct 1;15(19):5349-57.
Here we report the isolation of a cDNA encoding a new p53-associating protein. This new protein has been called MDMX on the basis of its structural similarity to MDM2, which is especially notable in the p53-binding domain. In addition, the putative metal binding domains in the C-terminal part of MDM2 are completely conserved in MDMX. The middle part of the MDMX and MDM2 proteins shows a low degree of conservation. We can show by co-immunoprecipitation that the MDMX protein interacts specifically with p53 in vivo. This interaction probably occurs with the N-terminal part of p53, because the activity of the transcription activation domain of p53 was inhibited by co-transfection of MDMX. Northern blotting showed that MDMX, like MDM2, is expressed in all tissues tested, and that several mRNAs for MDMX can be detected. Interestingly, the level of MDMX mRNA is unchanged after UV irradiation, in contrast to MDM2 transcription. This observation suggests that MDMX may be a differently regulated modifier of p53 activity in comparison with MDM2. Our study indicates that at least one additional member of the MDM protein family exists which can modulate p53 function.
在此我们报告了一种编码新型p53相关蛋白的cDNA的分离。基于其与MDM2在结构上的相似性,这种新蛋白被命名为MDMX,这在p53结合结构域中尤为显著。此外,MDM2 C末端部分的假定金属结合结构域在MDMX中完全保守。MDMX和MDM2蛋白的中间部分显示出较低程度的保守性。我们通过共免疫沉淀表明,MDMX蛋白在体内与p53特异性相互作用。这种相互作用可能发生在p53的N末端部分,因为MDMX的共转染抑制了p53转录激活结构域的活性。Northern印迹显示,与MDM2一样,MDMX在所有测试组织中均有表达,并且可以检测到几种MDMX的mRNA。有趣地是,与MDM2转录相反,紫外线照射后MDMX mRNA水平未发生变化。该观察结果表明,与MDM2相比,MDMX可能是一种受不同调控的p53活性调节因子。我们的研究表明,MDM蛋白家族至少还存在一个可以调节p53功能的成员。