Lazaris-Karatzas A, Montine K S, Sonenberg N
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Nature. 1990 Jun 7;345(6275):544-7. doi: 10.1038/345544a0.
Eukaryotic cellular mRNAs have a 5' cap structure (m7 GpppX) that facilitates binding to ribosomes and is required for efficient translation. A specific initiation factor, eIF-4F, mediates the function of the cap and consists of three subunits, one of which, eIF-4E, binds the cap. This subunit is present in limiting amounts in the cell, and is thought to be regulated by phosphorylation: decreased phosphorylation of eIF-4E following various treatments correlates with a decrease in cellular translation rate. These observations suggest that eIF-4E lies on the mitogenic signal transduction pathway, and we reasoned that overexpression of eIF-4E might profoundly affect cellular growth properties. We report here that overexpression of eIF-4E in NIH 3T3 and Rat 2 fibroblasts causes their tumorigenic transformation as determined by three criteria: formation of transformed foci on a monolayer of cells; anchorage-independent growth; and tumour formation in nude mice.
真核细胞信使核糖核酸(mRNA)具有5'帽结构(m7GpppX),该结构有助于与核糖体结合,是高效翻译所必需的。一种特定的起始因子eIF-4F介导帽的功能,它由三个亚基组成,其中一个亚基eIF-4E与帽结合。该亚基在细胞中的含量有限,并且被认为受磷酸化调节:各种处理后eIF-4E磷酸化的降低与细胞翻译速率的降低相关。这些观察结果表明eIF-4E位于促有丝分裂信号转导途径上,我们推测eIF-4E的过表达可能会深刻影响细胞生长特性。我们在此报告,通过三个标准确定,在NIH 3T3和大鼠2成纤维细胞中eIF-4E的过表达会导致它们发生致瘤性转化:在单层细胞上形成转化灶;不依赖贴壁生长;以及在裸鼠中形成肿瘤。