Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom.
Genes Dev. 2011 Sep 1;25(17):1770-82. doi: 10.1101/gad.17268411.
Polyadenylation [poly(A)] signals (PAS) are a defining feature of eukaryotic protein-coding genes. The central sequence motif AAUAAA was identified in the mid-1970s and subsequently shown to require flanking, auxiliary elements for both 3'-end cleavage and polyadenylation of premessenger RNA (pre-mRNA) as well as to promote downstream transcriptional termination. More recent genomic analysis has established the generality of the PAS for eukaryotic mRNA. Evidence for the mechanism of mRNA 3'-end formation is outlined, as is the way this RNA processing reaction communicates with RNA polymerase II to terminate transcription. The widespread phenomenon of alternative poly(A) site usage and how this interrelates with pre-mRNA splicing is then reviewed. This shows that gene expression can be drastically affected by how the message is ended. A central theme of this review is that while genomic analysis provides generality for the importance of PAS selection, detailed mechanistic understanding still requires the direct analysis of specific genes by genetic and biochemical approaches.
聚腺苷酸化 [poly(A)] 信号 (PAS) 是真核蛋白编码基因的一个定义特征。中央序列基序 AAUAAA 于 20 世纪 70 年代中期被发现,随后表明其需要侧翼辅助元件,以便对前信使 RNA (pre-mRNA) 进行 3'-末端切割和聚腺苷酸化,以及促进下游转录终止。最近的基因组分析已经确立了 PAS 对真核 mRNA 的普遍性。本文概述了 mRNA 3'-末端形成的机制证据,以及这种 RNA 加工反应如何与 RNA 聚合酶 II 进行通讯以终止转录。然后,还回顾了交替聚腺苷酸化位点使用的广泛现象,以及这与 pre-mRNA 剪接的关系。这表明,通过终止信息的方式可以极大地影响基因表达。本文的一个中心主题是,虽然基因组分析为 PAS 选择的重要性提供了普遍性,但详细的机制理解仍然需要通过遗传和生化方法直接分析特定基因。