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共转录前体mRNA剪接和3'端形成需要RNA聚合酶II羧基末端结构域磷酸化。

RNA polymerase II carboxy-terminal domain phosphorylation is required for cotranscriptional pre-mRNA splicing and 3'-end formation.

作者信息

Bird Gregory, Zorio Diego A R, Bentley David L

机构信息

Department of Biochemistry and Molecular Genetics, University of Colorado Health Science Center at Fitzsimons, P.O. Box 6511, Aurora, CO 80045, USA.

出版信息

Mol Cell Biol. 2004 Oct;24(20):8963-9. doi: 10.1128/MCB.24.20.8963-8969.2004.

Abstract

We investigated the role of RNA polymerase II (pol II) carboxy-terminal domain (CTD) phosphorylation in pre-mRNA processing coupled and uncoupled from transcription in Xenopus oocytes. Inhibition of CTD phosphorylation by the kinase inhibitors 5,6-dichloro-1beta-D-ribofuranosyl-benzimidazole and H8 blocked transcription-coupled splicing and poly(A) site cleavage. These experiments suggest that pol II CTD phosphorylation is required for efficient pre-mRNA splicing and 3'-end formation in vivo. In contrast, processing of injected pre-mRNA was unaffected by either kinase inhibitors or alpha-amanitin-induced depletion of pol II. pol II therefore does not appear to participate directly in posttranscriptional processing, at least in frog oocytes. Together these experiments show that the influence of the phosphorylated CTD on pre-mRNA splicing and 3'-end processing is mediated by transcriptional coupling.

摘要

我们研究了RNA聚合酶II(pol II)羧基末端结构域(CTD)磷酸化在非洲爪蟾卵母细胞中与转录偶联及非偶联的前体mRNA加工过程中的作用。激酶抑制剂5,6-二氯-1β-D-呋喃核糖基苯并咪唑和H8对CTD磷酸化的抑制作用阻断了转录偶联的剪接和聚腺苷酸化位点切割。这些实验表明,pol II CTD磷酸化是体内高效前体mRNA剪接和3'末端形成所必需的。相比之下,注射的前体mRNA的加工不受激酶抑制剂或α-鹅膏蕈碱诱导的pol II耗竭的影响。因此,pol II似乎不直接参与转录后加工,至少在蛙卵母细胞中是这样。这些实验共同表明,磷酸化的CTD对前体mRNA剪接和3'末端加工的影响是由转录偶联介导的。

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