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

被引:12
作者
Nikolaou, Nikolas [1 ,2 ]
Gordon, Patricia M. [1 ]
Hamid, Fursham [1 ]
Taylor, Richard [1 ]
Lloyd-Jones, Joshua [2 ]
Makeyev, Eugene V. [1 ]
Houart, Corinne [1 ]
机构
[1] Kings Coll London, Ctr Dev Neurobiol MRC CNDD, IoPPN, Guys Campus, London SE1 1UL, England
[2] Univ Bath, Dept Life Sci, Bath BA2 7AY, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
IN-VIVO; AGRIN; ZEBRAFISH; RECEPTOR; LOCALIZATION; EXPRESSION; REVEALS; COMPLEX; TRANSLATION; TRANSPOSON;
D O I
10.1016/j.cub.2022.10.048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 synaptogen-esis. This cytoplasmic pool has a protective role for a limited number of transcripts regulating their abun-dance 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, func-tion of non-nuclear SNRNP70 in axonal development, indicating a role of spliceosome proteins in cyto-plasmic RNA metabolism during neuronal connectivity.
引用
收藏
页码:5099 / +
页数:26
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