MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Curr Opin Struct Biol. 2019 Dec;59:143-150. doi: 10.1016/j.sbi.2019.08.001. Epub 2019 Sep 6.
The polyadenosine (poly(A)) tail found on the 3'-end of almost all eukaryotic mRNAs is important for mRNA stability and regulation of translation. mRNA 3'-end processing occurs co-transcriptionally and involves more than 20 proteins to specifically recognize the polyadenylation site, cleave the pre-mRNA, add a poly(A) tail, and trigger transcription termination. The polyadenylation site (PAS) defines the end of the 3'-untranslated region (3'-UTR) and, therefore, selection of the cleavage site is a critical event in regulating gene expression. Integrated structural biology approaches including biochemical reconstitution of multi-subunit complexes, cross-linking mass spectrometry, and structural analyses by X- ray crystallography and single-particle electron cryo-microscopy (cryoEM) have enabled recent progress in understanding the molecular mechanisms of the mRNA 3'-end processing machinery. Here, we describe new molecular insights into pre-mRNA recognition, cleavage and polyadenylation.
真核生物 mRNA 3' 端的多聚腺苷酸(poly(A))尾对于 mRNA 的稳定性和翻译调控非常重要。mRNA 3' 端加工是在转录过程中发生的,涉及 20 多种蛋白质来特异性识别多聚腺苷酸化位点,切割前体 RNA,添加 poly(A)尾,并触发转录终止。多聚腺苷酸化位点(PAS)定义了 3' 非翻译区(3'-UTR)的末端,因此,切割位点的选择是调节基因表达的关键事件。综合结构生物学方法,包括多亚基复合物的生化重建、交联质谱以及 X 射线晶体学和单颗粒电子 cryo-EM(cryoEM)结构分析,使得人们对 mRNA 3' 端加工机制的分子机制有了新的认识。在这里,我们描述了在 pre-mRNA 识别、切割和多聚腺苷酸化方面的新分子见解。