Scheper G C, Voorma H O, Thomas A A
Department of Molecular Cell Biology, The Netherlands.
J Biol Chem. 1992 Apr 15;267(11):7269-74.
Two mechanisms of initiation of protein synthesis are known. The 5' cap-dependent model requires the activity of cap-binding eukaryotic initiation factors (eIF)1-4E and -4F, inducing unwinding of mRNA secondary structures. The internal initiation model is 5' cap-independent and requires a ribosomal entry site formed by higher order structures of the mRNA. It has been proposed that this mechanism does not need eIF-4E and eIF-4F. We prepared bicistronic transcripts on which both mechanisms of initiation occur, allowing the determination of the initiation factor dependence of these two mechanisms simultaneously. The unwinding factors eIF-4A, eIF-4B, and eIF-4F were found to be necessary for 5' cap-dependent initiation as well as for internal initiation. Surprisingly, efficient translation of both cistrons on the bicistronic mRNA required eIF-4E. A model is presented in which assembly of eIF-4E into a functional eIF-4F complex is a prerequisite for both types of initiation.
已知蛋白质合成起始的两种机制。5'帽依赖性模型需要帽结合真核起始因子(eIF)1-4E和-4F的活性,诱导mRNA二级结构解旋。内部起始模型不依赖5'帽,需要由mRNA高阶结构形成的核糖体进入位点。有人提出这种机制不需要eIF-4E和eIF-4F。我们制备了双顺反子转录本,两种起始机制都在其上发生,从而能够同时确定这两种机制对起始因子的依赖性。发现解旋因子eIF-4A、eIF-4B和eIF-4F对于5'帽依赖性起始以及内部起始都是必需的。令人惊讶的是,双顺反子mRNA上两个顺反子的有效翻译都需要eIF-4E。提出了一个模型,其中eIF-4E组装成功能性eIF-4F复合物是两种起始类型的先决条件。