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生长停滞和DNA损伤诱导蛋白45α(Gadd45a)调节β-连环蛋白的分布并维持细胞间粘附/接触。

Gadd45a regulates beta-catenin distribution and maintains cell-cell adhesion/contact.

作者信息

Ji J, Liu R, Tong T, Song Y, Jin S, Wu M, Zhan Q

机构信息

State Key Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, PR China.

出版信息

Oncogene. 2007 Sep 27;26(44):6396-405. doi: 10.1038/sj.onc.1210469. Epub 2007 Apr 23.

DOI:10.1038/sj.onc.1210469
PMID:17452974
Abstract

Gadd45a, a growth arrest and DNA-damage gene, plays important roles in the control of cell cycle checkpoints, DNA repair and apoptosis. We show here that Gadd45a is involved in the control of cell contact inhibition and cell-cell adhesion. Gadd45a can serve as an adapter to enhance the interaction between beta-catenin and Caveolin-1, and in turn induces beta-catenin translocation to cell membrane for maintaining cell-cell adhesion/contact inhibition. This is coupled with reduction of beta-catenin in cytoplasm and nucleus following Gadd45a induction, which is reflected by the downregulation of cyclin D1, one of the beta-catenin targeted genes. Additionally, Gadd45a facilitates ultraviolet radiation-induced degradation of cytoplasmic and nuclear beta-catenin in a p53-dependent manner via activation of p38 kinase. These findings define a novel link that connects Gadd45a to cell-cell adhesion and cell contact inhibition, which might contribute to the role of Gadd45a in inhibiting tumorigenesis.

摘要

生长停滞和DNA损伤基因Gadd45a在细胞周期检查点控制、DNA修复和细胞凋亡中发挥重要作用。我们在此表明,Gadd45a参与细胞接触抑制和细胞间黏附的控制。Gadd45a可作为衔接蛋白增强β-连环蛋白与小窝蛋白-1之间的相互作用,进而诱导β-连环蛋白易位至细胞膜以维持细胞间黏附/接触抑制。这与Gadd45a诱导后细胞质和细胞核中β-连环蛋白的减少相关,这一点通过β-连环蛋白靶向基因之一细胞周期蛋白D1的下调得以体现。此外,Gadd45a通过激活p38激酶以p53依赖的方式促进紫外线辐射诱导的细胞质和细胞核β-连环蛋白降解。这些发现定义了一种将Gadd45a与细胞间黏附及细胞接触抑制联系起来的新关联,这可能有助于Gadd45a在抑制肿瘤发生中的作用。

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