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RBBP6将前体mRNA 3'末端加工锚定到核斑点以实现高效基因表达。

RBBP6 anchors pre-mRNA 3' end processing to nuclear speckles for efficient gene expression.

作者信息

Yoon Yoseop, Bournique Elodie, Soles Lindsey V, Yin Hong, Chu Hsu-Feng, Yin Christopher, Zhuang Yinyin, Liu Xiangyang, Liu Liang, Jeong Joshua, Yu Clinton, Valdez Marielle, Tian Lusong, Huang Lan, Shi Xiaoyu, Seelig Georg, Ding Fangyuan, Tong Liang, Buisson Rémi, Shi Yongsheng

机构信息

Department of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA.

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA.

出版信息

Mol Cell. 2025 Feb 6;85(3):555-570.e8. doi: 10.1016/j.molcel.2024.12.016. Epub 2025 Jan 10.

Abstract

Pre-mRNA 3' processing is an integral step in mRNA biogenesis. However, where this process occurs in the nucleus remains unknown. Here, we demonstrate that nuclear speckles (NSs), membraneless organelles enriched with splicing factors, are major sites for pre-mRNA 3' processing in human cells. We show that the essential pre-mRNA 3' processing factor retinoblastoma-binding protein 6 (RBBP6) associates strongly with NSs via its C-terminal intrinsically disordered region (IDR). Importantly, although the conserved N-terminal domain (NTD) of RBBP6 is sufficient for pre-mRNA 3' processing in vitro, its IDR-mediated association with NSs is required for efficient pre-mRNA 3' processing in cells. Through proximity labeling analyses, we provide evidence that pre-mRNA 3' processing for over 50% of genes occurs near NSs. We propose that NSs serve as hubs for RNA polymerase II transcription, pre-mRNA splicing, and 3' processing, thereby enhancing the efficiency and coordination of different gene expression steps.

摘要

前体mRNA 3'加工是mRNA生物合成过程中不可或缺的一步。然而,该过程在细胞核中的发生位置仍不清楚。在此,我们证明核斑点(NSs),即富含剪接因子的无膜细胞器,是人类细胞中前体mRNA 3'加工的主要场所。我们发现,重要的前体mRNA 3'加工因子视网膜母细胞瘤结合蛋白6(RBBP6)通过其C端内在无序区域(IDR)与核斑点紧密结合。重要的是,尽管RBBP6保守的N端结构域(NTD)在体外足以进行前体mRNA 3'加工,但在细胞中高效的前体mRNA 3'加工需要其IDR介导的与核斑点的结合。通过邻近标记分析,我们提供证据表明超过50%的基因的前体mRNA 3'加工发生在核斑点附近。我们提出,核斑点作为RNA聚合酶II转录、前体mRNA剪接和3'加工的枢纽,从而提高不同基因表达步骤的效率和协调性。

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