Suppr超能文献

U1剪接体蛋白SNRNP70的细胞质池塑造轴突转录组并调节运动连接性。

Cytoplasmic pool of U1 spliceosome protein SNRNP70 shapes the axonal transcriptome and regulates motor connectivity.

作者信息

Nikolaou Nikolas, Gordon Patricia M, Hamid Fursham, Taylor Richard, Lloyd-Jones Joshua, Makeyev Eugene V, Houart Corinne

机构信息

Centre for Developmental Neurobiology MRC CNDD, IoPPN, Guy's Campus, King's College London, London SE1 1UL, UK; Department of Life Sciences, University of Bath, Bath BA2 7AY, UK.

Centre for Developmental Neurobiology MRC CNDD, IoPPN, Guy's Campus, King's College London, London SE1 1UL, UK.

出版信息

Curr Biol. 2022 Dec 5;32(23):5099-5115.e8. doi: 10.1016/j.cub.2022.10.048. Epub 2022 Nov 15.

Abstract

Regulation of pre-mRNA splicing and polyadenylation plays a profound role in neurons by diversifying the proteome and modulating gene expression in response to physiological cues. Although most of the pre-mRNA processing is thought to occur in the nucleus, numerous splicing regulators are also found in neurites. Here, we show that U1-70K/SNRNP70, a component of the major spliceosome, localizes in RNA-associated granules in zebrafish axons. We identify the extra-nuclear SNRNP70 as an important regulator of motor axonal growth, nerve-dependent acetylcholine receptor (AChR) clustering, and neuromuscular synaptogenesis. This cytoplasmic pool has a protective role for a limited number of transcripts regulating their abundance and trafficking inside axons. Moreover, non-nuclear SNRNP70 regulates splice variants of transcripts such as agrin, thereby controlling synapse formation. Our results point to an unexpected, yet essential, function of non-nuclear SNRNP70 in axonal development, indicating a role of spliceosome proteins in cytoplasmic RNA metabolism during neuronal connectivity.

摘要

前体mRNA剪接和聚腺苷酸化的调控通过使蛋白质组多样化并响应生理信号调节基因表达,在神经元中发挥着深远作用。尽管大多数前体mRNA加工被认为发生在细胞核中,但在神经突中也发现了许多剪接调节因子。在这里,我们表明主要剪接体的一个组成部分U1-70K/SNRNP70定位于斑马鱼轴突中与RNA相关的颗粒中。我们确定核外SNRNP70是运动轴突生长、神经依赖性乙酰胆碱受体(AChR)聚集和神经肌肉突触形成的重要调节因子。这个细胞质池对有限数量的转录本具有保护作用,调节它们在轴突内的丰度和运输。此外,核外SNRNP70调节诸如聚集蛋白等转录本的剪接变体,从而控制突触形成。我们的结果指出了核外SNRNP70在轴突发育中意想不到但必不可少的功能,表明剪接体蛋白在神经元连接过程中细胞质RNA代谢中的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验