RNA剪接
磷酸化
选择性拼接
小核核糖核蛋白
细胞生物学
生物化学
化学
核糖核蛋白
生物
功能(生物学)
代谢途径
化学生物学
蛋白质剪接
异质核核糖核蛋白
剪接体
酶
蛋白质功能
新陈代谢
计算生物学
拼接因子
基因敲除
生物物理学
作者
Amaia Zabala‐Letona,Mikel Pujana-Vaquerizo,Belen Martinez-Laosa,María Ponce-Rodriguez,Saioa Garcia‐Longarte,Isabel Mendizabal,Ana Gimeno,Malgorzata Ewa Rogalska,Joycelyn Tan,Diana Cabrera,Sebastiaan van Liempd,Pilar Ximénez‐Embún,Sergio Espinosa,Maider Fagoaga-Eugui,Francesca Peccati,Maciej Zakrzewski,Ianire Astobiza,Mikel Arana-Castañares,Sarah Cherkaoui,Maria Sendino
出处
期刊:Nature
[Nature Portfolio]
日期:2026-01-14
卷期号:651 (8106): 819-828
被引量:8
标识
DOI:10.1038/s41586-025-09965-1
摘要
Metabolites are central to cellular homeostasis. Although much emphasis has been placed on their relevance to meet energetic and biosynthetic demands, metabolic intermediates also function as signalling molecules. Here we show that polyamines, small polycations that are critical to cellular homeostasis1–3, regulate the process of alternative pre-mRNA splicing. We find that inhibition of polyamine synthesis increases phosphorylation of spliceosomal proteins, concomitant with perturbation of alternative splicing in cells and tissues. Mechanistically, molecular modelling combined with biochemical assays revealed that polyamines bind to acidic phosphorylatable motifs in splicing factors of the U2 small nuclear ribonucleoprotein SF3 subcomplex, thus preventing the action of upstream kinases. We refer to this molecular process by which polyamines regulate protein phosphorylation as metabolic shielding. Polyamines prevent the action of kinases on acidic phosphorylatable motifs in spliceosomal proteins, thus providing a mechanism for metabolite-mediated regulation of alternative splicing in cells.
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