Mauro Vincent P, Chappell Stephen A, Dresios John
Department of Neurobiology, The Scripps Research Institute, La Jolla, California, USA.
Methods Enzymol. 2007;429:323-54. doi: 10.1016/S0076-6879(07)29015-9.
In eukaryotes, translation initiation involves recruitment of ribosomal subunits at either the 5' m7G cap structure or at an internal ribosome entry site (IRES). For most mRNAs, the initiation codon is located some distance downstream, necessitating ribosomal movement to this site. Although the mechanistic details of this movement remain to be fully resolved, it appears to be nonlinear for some mRNAs (i.e., ribosomal subunits appear to bypass [shunt] segments of the 5' leader as they move to the initiation codon). This chapter describes various experimental approaches to assess ribosomal shunting and to identify mRNA elements (shunt sites) that facilitate shunting. In addition, we provide an overview of approaches that can be used to investigate the mechanism used by individual shunt sites, along with a detailed protocol for investigating putative base pairing interactions between shunt sites and 18S rRNA.
在真核生物中,翻译起始涉及核糖体亚基在5' m7G帽结构或内部核糖体进入位点(IRES)处的募集。对于大多数mRNA而言,起始密码子位于下游一段距离处,这就需要核糖体移动到该位点。尽管这种移动的机制细节仍有待完全阐明,但对于某些mRNA来说,它似乎是非线性的(即核糖体亚基在移向起始密码子的过程中似乎会绕过5'前导序列的某些片段)。本章描述了评估核糖体跳跃以及鉴定促进跳跃的mRNA元件(跳跃位点)的各种实验方法。此外,我们概述了可用于研究单个跳跃位点所使用机制的方法,以及用于研究跳跃位点与18S rRNA之间假定碱基配对相互作用的详细方案。