生物
RNA剪接
内含子
核糖核酸
基因
遗传学
下调和上调
细胞器
计算生物学
Rna处理
反式剪接
斑点图案
细胞生物学
选择性拼接
基因表达
RNA结合蛋白
信使核糖核酸
外显子
细胞核
小核RNA
基因表达调控
小RNA
拼接因子
RNA序列
snRNP公司
基因组
前体mRNA
作者
Michał Małszycki,Lisa Martina,İbrahim Avşar Ilık,Daniela Salgado Figueroa,Nirmalya Dasgupta,Mensura Feray Çoşar,Keun-Tae Kim,Gil Carraco,Beatrix Fauler,David Meierhofer,Thorsten Mielke,Hiroo Imai,Cantas Alev,Ferhat Ay,Tugce Uslu Aktas
出处
期刊:Cell
[Cell Press]
日期:2026-02-25
卷期号:189 (7): 2024-2039.e25
被引量:6
标识
DOI:10.1016/j.cell.2026.01.011
摘要
Nuclear speckles are conserved, membrane-less organelles linked to various post-transcriptional processes. Here, we examined their roles in human cells by engineered, acute removal of SON and SRRM2, two conserved speckle core components characterized by intrinsically disordered regions (IDRs). Their removal results in a significant downregulation of GC-rich genes with short introns clustered within GC-rich isochores, caused by inefficient and chaotic splicing; in contrast, the expression or splicing of genes outside these isochores remains unaffected. Comparative analysis across eukaryotes, from fungi to mammals, reveals that both GC-rich isochores and speckles are found exclusively in amniotes; moreover, the IDRs of SON have undergone notable expansion in the latter. Together, these findings suggest that the expansion of IDRs in vertebrates facilitated an increase in GC content by creating a condensate essential for splicing the by-products of this process: GC-rich, leveled exon-intron architectures.
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