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转录过程中剪接机制的差异募集预测全基因组范围内的mRNA剪接模式。

Differential recruitment of the splicing machinery during transcription predicts genome-wide patterns of mRNA splicing.

作者信息

Moore Michael J, Schwartzfarb Elissa M, Silver Pamela A, Yu Michael C

机构信息

Department of Systems Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Mol Cell. 2006 Dec 28;24(6):903-15. doi: 10.1016/j.molcel.2006.12.006.

Abstract

The splicing machinery associates with genes to facilitate efficient cotranscriptional mRNA processing. We have mapped these associations by genome localization analysis to ascertain how splicing is achieved and regulated on a system-wide scale. Our data show that factors important for intron recognition sample nascent mRNAs and are retained specifically at intron-containing genes via RNA-dependent interactions. Spliceosome assembly proceeds cotranscriptionally but completes posttranscriptionally in most cases. Some intron-containing genes were not bound by the spliceosome, including several developmentally regulated genes. On this basis, we predicted and verified regulated splicing and observed a role for nuclear mRNA surveillance in monitoring those events. Finally, we present evidence that cotranscriptional processing events determine the recruitment of specific mRNA export factors. Broadly, our results provide mechanistic insights into the coordinated regulation of transcription, mRNA processing, and nuclear export in executing complex gene expression programs.

摘要

剪接机制与基因相关联,以促进高效的共转录mRNA加工。我们通过基因组定位分析绘制了这些关联,以确定在全系统范围内剪接是如何实现和调控的。我们的数据表明,对内含子识别重要的因子会对新生mRNA进行取样,并通过RNA依赖性相互作用特异性地保留在含内含子的基因处。剪接体组装在转录过程中进行,但在大多数情况下在转录后完成。一些含内含子的基因未被剪接体结合,包括几个受发育调控的基因。在此基础上,我们预测并验证了调控剪接,并观察到核mRNA监测在监测这些事件中的作用。最后,我们提供证据表明共转录加工事件决定了特定mRNA输出因子的募集。广泛地说,我们的结果为执行复杂基因表达程序时转录、mRNA加工和核输出的协调调控提供了机制性见解。

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