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出人意料的结局:非规范的 3' 末端加工机制。

An unexpected ending: noncanonical 3' end processing mechanisms.

机构信息

Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

RNA. 2010 Feb;16(2):259-66. doi: 10.1261/rna.1907510. Epub 2009 Dec 9.

Abstract

Proper 3' end processing of a nascent transcript is critical for the functionality of the mature RNA. Although it has long been thought that virtually all long RNA polymerase II transcripts terminate in a poly(A) tail that is generated by endonucleolytic cleavage followed by polyadenylation, noncanonical 3' end processing mechanisms have recently been identified at several gene loci. Unexpectedly, enzymes with well-characterized roles in other RNA processing events, such as tRNA biogenesis and pre-mRNA splicing, cleave these nascent transcripts to generate their mature 3' ends despite the presence of nearby polyadenylation signals. In fact, the presence of multiple potential 3' end cleavage sites is the norm at many human genes, and recent work suggests that the choice among sites is regulated during development and in response to cellular cues. It is, therefore, becoming increasing clear that the selection of a proper 3' end cleavage site represents an important step in the regulation of gene expression and that the mature 3' ends of RNA polymerase II transcripts can be generated via multiple mechanisms.

摘要

新生转录本的正确 3' 端加工对于成熟 RNA 的功能至关重要。尽管长期以来人们一直认为,几乎所有的长 RNA 聚合酶 II 转录本都终止于多聚(A)尾,该多聚(A)尾是通过内切核酸酶切割后再加上多聚腺苷酸生成的,但最近在几个基因座中已经确定了非典型的 3' 端加工机制。出乎意料的是,在其他 RNA 加工事件中具有明确作用的酶,如 tRNA 生物发生和前体 mRNA 剪接,会切割这些新生转录本,生成其成熟的 3' 端,尽管附近存在多聚腺苷酸化信号。事实上,在许多人类基因中,多个潜在的 3' 端切割位点是正常的,最近的研究表明,在发育过程中和响应细胞信号时,位点之间的选择是受到调控的。因此,越来越明显的是,选择正确的 3' 端切割位点是基因表达调控的重要步骤,RNA 聚合酶 II 转录本的成熟 3' 端可以通过多种机制生成。

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