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本文引用的文献

1
Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination.人源 Senataxin 通过降解转录暂停位点形成的 RNA/DNA 杂交体促进 Xrn2 依赖的终止。
Mol Cell. 2011 Jun 24;42(6):794-805. doi: 10.1016/j.molcel.2011.04.026.
2
RNA polymerase II kinetics in polo polyadenylation signal selection.Polo 多聚腺苷酸化信号选择中的 RNA 聚合酶 II 动力学。
EMBO J. 2011 May 20;30(12):2431-44. doi: 10.1038/emboj.2011.156.
3
Unravelling the means to an end: RNA polymerase II transcription termination.揭示终点的手段:RNA 聚合酶 II 转录终止。
Nat Rev Mol Cell Biol. 2011 May;12(5):283-94. doi: 10.1038/nrm3098. Epub 2011 Apr 13.
4
Differential genome-wide profiling of tandem 3' UTRs among human breast cancer and normal cells by high-throughput sequencing.高通量测序分析人类乳腺癌细胞和正常细胞中串联 3'UTR 的差异全基因组图谱。
Genome Res. 2011 May;21(5):741-7. doi: 10.1101/gr.115295.110. Epub 2011 Apr 7.
5
Transcriptional activators enhance polyadenylation of mRNA precursors.转录激活因子增强 mRNA 前体的多聚腺苷酸化。
Mol Cell. 2011 Feb 18;41(4):409-18. doi: 10.1016/j.molcel.2011.01.022.
6
Alternative mRNA polyadenylation in eukaryotes: an effective regulator of gene expression.真核生物中的替代 mRNA 多聚腺苷酸化:一种有效的基因表达调控因子。
Wiley Interdiscip Rev RNA. 2011 Jan-Feb;2(1):23-31. doi: 10.1002/wrna.47.
7
Yeast Sen1 helicase protects the genome from transcription-associated instability.酵母 Sen1 解旋酶可保护基因组免受转录相关的不稳定性影响。
Mol Cell. 2011 Jan 7;41(1):21-32. doi: 10.1016/j.molcel.2010.12.007.
8
Comprehensive polyadenylation site maps in yeast and human reveal pervasive alternative polyadenylation.酵母和人类的综合多聚腺苷酸化位点图谱揭示了普遍存在的可变多聚腺苷酸化。
Cell. 2010 Dec 10;143(6):1018-29. doi: 10.1016/j.cell.2010.11.020.
9
Formation, regulation and evolution of Caenorhabditis elegans 3'UTRs.秀丽隐杆线虫 3'UTR 的形成、调控和进化。
Nature. 2011 Jan 6;469(7328):97-101. doi: 10.1038/nature09616. Epub 2010 Nov 17.
10
Crosstalk between mRNA 3' end processing and transcription initiation.mRNA 3' 端加工与转录起始的串扰。
Mol Cell. 2010 Nov 12;40(3):410-22. doi: 10.1016/j.molcel.2010.10.012.

结束信息:多聚(A)信号,过去和现在。

Ending the message: poly(A) signals then and now.

机构信息

Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom.

出版信息

Genes Dev. 2011 Sep 1;25(17):1770-82. doi: 10.1101/gad.17268411.

DOI:10.1101/gad.17268411
PMID:21896654
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3175714/
Abstract

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.

摘要

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。