Ustyantsev I G, Golubchikova J S, Borodulina O R, Kramerov D A
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, 119991 Russia.
Mol Biol (Mosk). 2017 Mar-Apr;51(2):262-273. doi: 10.7868/S0026898417010189.
Polyadenylation is the non-template addition of adenosine nucleotides at the 3'-end of RNA, which occurs after transcription and generates a poly(A) tail up to 250-300 nucleotides long. In the first section of our review, we consider the classical process of mRNA 3'-terminus formation, which involves the cleavage of the transcript synthesized by RNA polymerase II and the associated poly(A) tail synthesis by canonical polyadenylate polymerase. Nucleotide sequences needed for mRNA cleavage and poly(A) tail synthesis, in particular the AAUAAA polyadenylation signal, as well as numerous proteins and their complexes involved in mRNA cleavage and polyadenylation, is described in detail. The significance of the poly(A) tail for prolonging mRNA lifetime and stimulating their translation is discussed. Data presented in the second section demonstrate that RNA transcribed by RNA polymerase III from certain SINEs (Short Interspersed Elements) can undergo AAUAAA-dependent polyadenylation. The structural and functional features of RNA polymerase III determine the unusual character of polyadenylation of RNAs synthesized by this enzyme. The history of recent developments in this area of study have been described in greater detail, in particular the discovery of AAUAAA-dependent polyadenylation of RNA synthesized by RNA polymerase III, which has not been discussed previously. Data on AAUAAA-independent polyadenylation catalyzed by noncanonical TRAMP poly(A)-polymerases (Trf4 and Trf5) have been presented in the third section. These enzymes promote rapid degradation of RNAs by adding a short poly(A) tail to them. This mechanism enables the recognition, poly(A)-marking, and elimination of incorrectly folded noncoding transcripts (e.g. ribosomal and transfer RNAs).
多聚腺苷酸化是在RNA的3'末端非模板性地添加腺苷核苷酸,这一过程发生在转录之后,并产生一条长达250 - 300个核苷酸的多聚(A)尾。在我们综述的第一部分,我们考虑mRNA 3'末端形成的经典过程,该过程涉及RNA聚合酶II合成的转录本的切割以及由经典多聚腺苷酸聚合酶进行的相关多聚(A)尾合成。详细描述了mRNA切割和多聚(A)尾合成所需的核苷酸序列,特别是AAUAAA多聚腺苷酸化信号,以及参与mRNA切割和多聚腺苷酸化的众多蛋白质及其复合物。讨论了多聚(A)尾对于延长mRNA寿命和刺激其翻译的重要性。第二部分呈现的数据表明,RNA聚合酶III转录的某些短散在元件(SINEs)的RNA可进行依赖AAUAAA的多聚腺苷酸化。RNA聚合酶III的结构和功能特征决定了该酶合成的RNA多聚腺苷酸化的独特性质。该研究领域近期进展的历史已更详细地描述,特别是RNA聚合酶III合成的RNA依赖AAUAAA的多聚腺苷酸化的发现,此前尚未对此进行讨论。第三部分呈现了由非经典TRAMP多聚(A)聚合酶(Trf4和Trf5)催化的不依赖AAUAAA的多聚腺苷酸化的数据。这些酶通过给RNA添加一条短的多聚(A)尾来促进RNA的快速降解。这种机制能够识别、多聚(A)标记并消除折叠错误的非编码转录本(如核糖体RNA和转运RNA)。