Rousseau D, Gingras A C, Pause A, Sonenberg N
Department of Biochemistry and McGill Cancer Center, McGill University, Montreal, Quebec, Canada.
Oncogene. 1996 Dec 5;13(11):2415-20.
Initiation in eukaryotes is the rate limiting step of translation. The binding of the mRNA to the 40S ribosomal subunit, which is mediated by the mRNA cap structure, is a key target for control of protein synthesis. The cap binding protein, eIF4E, is the most limiting of all initiation factors and its overexpression in NIH3T3 cells causes malignant transformation. 4E-binding protein 1 (BP1) and 4E-BP2 are small proteins that bind to eIF4E and inhibit translation. Here, 4E-BPs were expressed in cells transformed by eIF4E or by v-src to determine the effect of 4E-BPs on cell growth and tumorigenicity. We show that 4E-BPs cause a significant reversion of the transformed phenotype. Thus, we demonstrate that the eIF4E-binding proteins act as negative regulators of cell growth. We propose that 4E-BPs are members of a class of negative regulators of cell growth acting on the translation machinery of the cell.
真核生物中的起始阶段是翻译的限速步骤。mRNA与40S核糖体亚基的结合由mRNA帽结构介导,是控制蛋白质合成的关键靶点。帽结合蛋白eIF4E是所有起始因子中最具限制性的,其在NIH3T3细胞中的过表达会导致恶性转化。4E结合蛋白1(BP1)和4E-BP2是与eIF4E结合并抑制翻译的小蛋白。在此,4E-BP在由eIF4E或v-src转化的细胞中表达,以确定4E-BP对细胞生长和致瘤性的影响。我们发现4E-BP可导致转化表型的显著逆转。因此,我们证明eIF4E结合蛋白作为细胞生长的负调节因子发挥作用。我们提出4E-BP是作用于细胞翻译机制的一类细胞生长负调节因子的成员。