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