期刊
PROTEIN & CELL
卷 14, 期 5, 页码 318-336出版社
OXFORD UNIV PRESS
DOI: 10.1093/procel/pwac008
关键词
SNIP1; RNPS1; spliceosome; detained intron; neurodegeneration
类别
Emerging evidence suggests that intron-detaining transcripts (IDTs) play a crucial role in cellular response to environmental stimuli and stress. This study proposes a mechanism for the splicing of detained introns (DIs) involving the interaction between Smad Nuclear Interacting Protein 1 (SNIP1) and RNPS1. The misregulation of this mechanism may contribute to neurodegeneration.
Emerging evidence suggests that intron-detaining transcripts (IDTs) are a nucleus-detained and polyadenylated mRNA pool for cell to quickly and effectively respond to environmental stimuli and stress. However, the underlying mechanisms of detained intron (DI) splicing are still largely unknown. Here, we suggest that post-transcriptional DI splicing is paused at the B-act state, an active spliceosome but not catalytically primed, which depends on Smad Nuclear Interacting Protein 1 (SNIP1) and RNPS1 (a serine-rich RNA binding protein) interaction. RNPS1 and B-act components preferentially dock at DIs and the RNPS1 docking is sufficient to trigger spliceosome pausing. Haploinsufficiency of Snip1 attenuates neurodegeneration and globally rescues IDT accumulation caused by a previously reported mutant U2 snRNA, a basal spliceosomal component. Snip1 conditional knockout in the cerebellum decreases DI splicing efficiency and causes neurodegeneration. Therefore, we suggest that SNIP1 and RNPS1 form a molecular brake to promote spliceosome pausing, and that its misregulation contributes to neurodegeneration.
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