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转录组图谱的 mRNP 生物发生因子定义了前 mRNA 的识别。

Transcriptome maps of mRNP biogenesis factors define pre-mRNA recognition.

机构信息

Max-Planck-Institute for Biophysical Chemistry, Am Faßberg 11, 37077 Göttingen, Germany.

Gene Center Munich and Department of Biochemistry, Center for Integrated Protein Science CIPSM, Ludwig-Maximilians-Universität München, Feodor-Lynen-Straße 25, 81377 Munich, Germany.

出版信息

Mol Cell. 2014 Sep 4;55(5):745-57. doi: 10.1016/j.molcel.2014.08.005.

Abstract

Biogenesis of eukaryotic messenger ribonucleoprotein complexes (mRNPs) involves the synthesis, splicing, and 3' processing of pre-mRNA, and the assembly of mature mRNPs for nuclear export. We mapped 23 mRNP biogenesis factors onto the yeast transcriptome, providing 10(4)-10(6) high-confidence RNA interaction sites per factor. The data reveal how mRNP biogenesis factors recognize pre-mRNA elements in vivo. They define conserved interactions between splicing factors and pre-mRNA introns, including the recognition of intron-exon junctions and the branchpoint. They also identify a unified arrangement of 3' processing factors at pre-mRNA polyadenylation (pA) sites in yeast and human, which results from an A-U sequence bias at pA sites. Global data analysis indicates that 3' processing factors have roles in splicing and RNA surveillance, and that they couple mRNP biogenesis events to restrict nuclear export to mature mRNPs.

摘要

真核信使核糖核蛋白复合物(mRNP)的生物发生涉及前体 mRNA 的合成、剪接和 3' 加工,以及成熟 mRNP 用于核输出的组装。我们将 23 种 mRNP 生物发生因子映射到酵母转录组上,每个因子提供 10(4)-10(6)个高置信度的 RNA 相互作用位点。这些数据揭示了 mRNP 生物发生因子如何在体内识别前体 mRNA 元件。它们定义了剪接因子与前体 mRNA 内含子之间的保守相互作用,包括内含子-外显子接头和分支点的识别。它们还鉴定了酵母和人类中 3' 加工因子在 pre-mRNA 多聚腺苷酸化 (pA) 位点的统一排列,这是由于 pA 位点处的 A-U 序列偏倚所致。全局数据分析表明,3' 加工因子在剪接和 RNA 监测中具有作用,并且它们将 mRNP 生物发生事件与限制核输出到成熟 mRNP 相关联。

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