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DEAD盒蛋白Ddx42p调节凋亡刺激因子ASPP2的功能。

The DEAD box protein Ddx42p modulates the function of ASPP2, a stimulator of apoptosis.

作者信息

Uhlmann-Schiffler H, Kiermayer S, Stahl H

机构信息

Department of Medical Biochemistry and Molecular Biology, The Saarland University, Homburg, Germany.

出版信息

Oncogene. 2009 May 21;28(20):2065-73. doi: 10.1038/onc.2009.75. Epub 2009 Apr 20.

Abstract

Ddx42p is a recently characterized mammalian DEAD box protein with unknown cellular function. We found that in human cells Ddx42p physically interacts with ASPP2, a major apoptosis inducer known to enhance p53 transactivation of proapoptotic genes. The proteins interact via a domain within the carboxy-terminal part of Ddx42p and a mid-amino-terminal sequence as well as the ankyrin-SH3 region of ASPP2. Overexpression of Ddx42p interferes with apoptosis induction by ASPP2, whereas Ddx42p knockdown reduces the survival rate of cultured human cells. In addition, ASPP2 is found in cytoplasm and nucleus at low Ddx42p level, and predominantly in cytoplasm at high concentration of Ddx42p, respectively. Our results show that Ddx42p is capable of modulating ASPP2 function.

摘要

Ddx42p是一种最近被鉴定出的哺乳动物DEAD盒蛋白,其细胞功能未知。我们发现,在人类细胞中,Ddx42p与ASPP2发生物理相互作用,ASPP2是一种主要的凋亡诱导因子,已知可增强p53对促凋亡基因的反式激活作用。这两种蛋白质通过Ddx42p羧基末端部分的一个结构域、ASPP2中氨基末端序列以及锚蛋白-SH3区域相互作用。Ddx42p的过表达会干扰ASPP2诱导的凋亡,而敲低Ddx42p则会降低培养的人类细胞的存活率。此外,在低水平Ddx42p时,ASPP2分别存在于细胞质和细胞核中,而在高浓度Ddx42p时,ASPP2主要存在于细胞质中。我们的结果表明,Ddx42p能够调节ASPP2的功能。

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