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共转录前体 mRNA 剪接中新兴和再现的主题。

Emerging and re-emerging themes in co-transcriptional pre-mRNA splicing.

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.

出版信息

Mol Cell. 2024 Oct 3;84(19):3656-3666. doi: 10.1016/j.molcel.2024.08.036.

Abstract

Proper gene expression requires the collaborative effort of multiple macromolecular machines to produce functional messenger RNA. As RNA polymerase II (RNA Pol II) transcribes DNA, the nascent pre-messenger RNA is heavily modified by other complexes such as 5' capping enzymes, the spliceosome, the cleavage, and polyadenylation machinery as well as RNA-modifying/editing enzymes. Recent evidence has demonstrated that pre-mRNA splicing and 3' end cleavage can occur on similar timescales as transcription and significantly cross-regulate. In this review, we discuss recent advances in co-transcriptional processing and how it contributes to gene regulation. We highlight how emerging areas-including coordinated splicing events, physical interactions between the RNA synthesis and modifying machinery, rapid and delayed splicing, and nuclear organization-impact mRNA isoforms. Coordination among RNA-processing choices yields radically different mRNA and protein products, foreshadowing the likely regulatory importance of co-transcriptional RNA folding and co-transcriptional modifications that have yet to be characterized in detail.

摘要

正确的基因表达需要多种大分子机器的协同作用,以产生功能性信使 RNA。当 RNA 聚合酶 II(RNA Pol II)转录 DNA 时,新生的前信使 RNA 会被其他复合物(如 5' 加帽酶、剪接体、切割和多聚腺苷酸化机器以及 RNA 修饰/编辑酶)进行大量修饰。最近的证据表明,前 mRNA 剪接和 3' 端切割可以与转录同时发生,并显著相互调节。在这篇综述中,我们讨论了转录共加工的最新进展及其对基因调控的贡献。我们强调了包括协调剪接事件、RNA 合成和修饰机制之间的物理相互作用、快速和延迟剪接以及核组织在内的新兴领域如何影响 mRNA 异构体。RNA 加工选择之间的协调产生了截然不同的 mRNA 和蛋白质产物,预示着 RNA 折叠和转录共修饰的可能调控重要性,这些仍有待详细描述。

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