Haimov Ora, Sinvani Hadar, Dikstein Rivka
Dept. of Biological Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel.
Dept. of Biological Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel.
Biochim Biophys Acta. 2015 Nov;1849(11):1313-8. doi: 10.1016/j.bbagrm.2015.09.006. Epub 2015 Sep 14.
Eukaryotic translation initiation is an intricate and multi-step process that includes 43S Pre-Initiation Complex (PIC) assembly, attachment of the PIC to the mRNA, scanning, start codon selection and 60S subunit joining. Translation initiation of most mRNAs involves recognition of a 5'end m7G cap and ribosomal scanning in which the 5' UTR is checked for complementarity with the AUG. There is however an increasing number of mRNAs directing translation initiation that deviate from the predominant mechanism. In this review we summarize the canonical translation initiation process and describe non-canonical mechanisms that are cap-dependent but operate without scanning. In particular we focus on several examples of translation initiation driven either by mRNAs with extremely short 5' leaders or by highly complex 5' UTRs that promote ribosome shunting.
真核生物翻译起始是一个复杂的多步骤过程,包括43S前起始复合物(PIC)组装、PIC与mRNA的结合、扫描、起始密码子选择以及60S亚基的加入。大多数mRNA的翻译起始涉及对5'端m7G帽的识别和核糖体扫描,其中会检查5'非翻译区(UTR)与AUG的互补性。然而,越来越多指导翻译起始的mRNA偏离了主要机制。在本综述中,我们总结了经典的翻译起始过程,并描述了不依赖扫描但依赖帽的非经典机制。特别是,我们重点关注了由具有极短5'前导序列的mRNA或促进核糖体跳跃的高度复杂5'UTR驱动的几个翻译起始例子。