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爱泼斯坦-巴尔病毒潜伏膜蛋白1对ras-MAPK依赖途径的激活是细胞转化所必需的。

Activation of a ras-MAPK-dependent pathway by Epstein-Barr virus latent membrane protein 1 is essential for cellular transformation.

作者信息

Roberts M L, Cooper N R

机构信息

Department of Immunology, Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

Virology. 1998 Jan 5;240(1):93-9. doi: 10.1006/viro.1997.8901.

Abstract

The latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) is the only EBV protein which possesses the properties of an oncogene. In studies initiated to evaluate the mechanisms involved in EBV-induced malignant transformation, the extracellular response kinase (ERK) 1/2 were found to be activated 2 days after EBV infection of purified resting human B cells. Transfection studies in Rat-1 fibroblasts, an established rodent cell line, showed that LMP1 mediates ERK 1/2 activation. Cotransfection experiments with a dominant negative ras mutant demonstrated that such MAPK activation occurs via a ras-dependent pathway. Finally, cotransfection studies showed that ras activation is required for LMP-1-mediated malignant transformation of Rat-1 cells.

摘要

爱泼斯坦-巴尔病毒(EBV)的潜伏膜蛋白1(LMP1)是唯一具有癌基因特性的EBV蛋白。在为评估EBV诱导恶性转化所涉及机制而开展的研究中,发现纯化的静息人B细胞在感染EBV两天后,细胞外信号调节激酶(ERK)1/2被激活。在已建立的啮齿动物细胞系大鼠-1成纤维细胞中进行的转染研究表明,LMP1介导ERK 1/2的激活。用显性负性ras突变体进行的共转染实验表明,这种丝裂原活化蛋白激酶(MAPK)激活是通过ras依赖途径发生的。最后,共转染研究表明,ras激活是LMP-1介导大鼠-1细胞恶性转化所必需的。

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