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RNA聚合酶II的C末端结构域有助于确保GluR-B转录本的编辑先于剪接。

The C-terminal domain of RNA Pol II helps ensure that editing precedes splicing of the GluR-B transcript.

作者信息

Ryman Kicki, Fong Nova, Bratt Eva, Bentley David L, Ohman Marie

机构信息

Department of Molecular Biology and Functional Genomics, Stockholm University, Stockholm, Sweden.

出版信息

RNA. 2007 Jul;13(7):1071-8. doi: 10.1261/rna.404407. Epub 2007 May 24.

Abstract

The C-terminal domain (CTD) of the large subunit of RNA polymerase II (Pol II) influences many steps in the synthesis of an mRNA and helps control the final destiny of the mature transcript. ADAR2 edits RNA by converting adenosine to inosine within double-stranded or structured RNA. Site-selective A-to-I editing often occurs at sites near exon/intron borders, where it depends on intronic sequences for substrate recognition. It is therefore essential that editing precedes splicing. We have investigated whether there is coordination between ADAR2 editing and splicing of the GluR-B pre-mRNA. We show that the CTD is required for efficient editing at the R/G site one base upstream of a 5'-splice site. The results suggest that the CTD enhances editing at the R/G site by preventing premature splicing that would remove the intronic recognition sites for ADAR2. Editing at the GluR-B Q/R site, 24 bases upstream of the intron 11 5'-splice site, stimulates splicing at this intron. Furthermore, unlike previously studied introns, the CTD actually inhibits excision of intron 11, which includes the complementary recognition sequences for the Q/R editing site. In summary, these results show that the CTD and ADAR2 function together to enforce the order of events that allows editing to precede splicing, and they furthermore suggest a new role for the CTD as a coordinator of two interdependent pre-mRNA processing events.

摘要

RNA聚合酶II(Pol II)大亚基的C末端结构域(CTD)影响mRNA合成的多个步骤,并有助于控制成熟转录本的最终命运。ADAR2通过将双链或结构化RNA中的腺苷转化为肌苷来编辑RNA。位点选择性A到I编辑通常发生在外显子/内含子边界附近的位点,在这些位点,它依赖内含子序列进行底物识别。因此,编辑先于剪接至关重要。我们研究了ADAR2编辑与GluR-B前体mRNA剪接之间是否存在协调。我们发现,CTD是在5'剪接位点上游一个碱基处的R/G位点进行高效编辑所必需的。结果表明,CTD通过防止过早剪接来增强R/G位点的编辑,而过早剪接会去除ADAR2的内含子识别位点。在第11内含子5'剪接位点上游24个碱基处的GluR-B Q/R位点进行编辑,会刺激该内含子的剪接。此外,与之前研究的内含子不同,CTD实际上抑制了第11内含子的切除,该内含子包含Q/R编辑位点的互补识别序列。总之,这些结果表明,CTD和ADAR2共同作用以确保编辑先于剪接的事件顺序,并且它们还暗示了CTD作为两个相互依赖的前体mRNA加工事件协调者的新作用。

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