a CNRS , Architecture et Réactivité de l'ARN UPR9002, Université de Strasbourg , Strasbourg , France.
b Laboratory of Regulation of Gene Expression, Institute of Microbiology ASCR , Prague , Czech Republic.
RNA Biol. 2017 Oct 3;14(10):1279-1285. doi: 10.1080/15476286.2016.1269993. Epub 2017 May 12.
For many years initiation and termination of mRNA translation have been studied separately. However, a direct link between these 2 isolated stages has been suggested by the fact that some initiation factors also control termination and can even promote ribosome recycling; i.e. the last stage where post-terminating 80S ribosomes are split to start a new round of initiation. Notably, it is now firmly established that, among other factors, ribosomal recycling critically requires the NTPase ABCE1. However, several earlier reports have proposed that ABCE1 also somehow participates in the initiation complex assembly. Based on an extended analysis of our recently published late-stage 48S initiation complex from rabbit, here we provide new mechanistic insights into this putative role of ABCE1 in initiation. This point of view represents the first structural evidence in which the regulatory role of the recycling factor ABCE1 in initiation is discussed and establishes a corner stone for elucidating the interplay between ABCE1 and several initiation factors during the transit from ribosomal recycling to formation of the elongation competent 80S initiation complex.
多年来,mRNA 翻译的起始和终止一直是分别研究的。然而,一些起始因子也控制终止,甚至可以促进核糖体循环,这一事实表明这两个独立的阶段之间存在直接联系;即终止后 80S 核糖体分裂以开始新一轮起始的最后阶段。值得注意的是,现在已经确定,除其他因素外,核糖体循环还严重依赖于 NTPase ABCE1。然而,早些时候的几项报道提出,ABCE1 也以某种方式参与起始复合物的组装。基于对我们最近发表的兔晚期 48S 起始复合物的扩展分析,我们在这里提供了关于 ABCE1 在起始中这种假定作用的新的机制见解。这种观点代表了第一个讨论了循环因子 ABCE1 在起始中的调节作用的结构证据,并为阐明 ABCE1 和几个起始因子在从核糖体循环到形成延伸能力的 80S 起始复合物的过渡过程中的相互作用奠定了基石。