生物
snRNP公司
细胞生物学
组蛋白
组蛋白H2A
遗传学
RNA剪接
基因
核糖核酸
作者
Shuying He,Pin Lyu,Marnie W. Skinner,Anthony Desotell,Brendan Foley,Chance M McCaig,Wei Wang,Qian Jiang,Liang Tong,William F. Marzluff,Michael J. Matunis
出处
期刊:Genes & Development
[Cold Spring Harbor Laboratory Press]
日期:2025-07-10
卷期号:39 (19-20): 1182-1197
标识
DOI:10.1101/gad.352728.125
摘要
Histone mRNAs are the only nonpolyadenylated mRNAs in eukaryotic cells and require specialized processing in the histone locus body (HLB), a nuclear body where essential processing factors, including the U7 snRNP, are concentrated. Recent studies have revealed that misregulation of histone pre-mRNA processing can lead to polyadenylation of histone mRNAs and disruption of histone protein homeostasis. Despite links to human disease, the factors contributing to polyadenylation of histone mRNAs and the mechanisms underlying HLB assembly and U7 snRNP biogenesis remain unclear. Here, we report novel functions of the small ubiquitin-related modifier 2 (SUMO2) in promoting histone pre-mRNA processing. Using a SUMO2 knockout osteosarcoma cell line, we identified a defect in 3′ end cleavage and a global increase in histone mRNA polyadenylation. Subsequent analysis of HLBs revealed increased dynamics and reduced levels of the U7 snRNP complex. By overexpressing the U7 snRNP-specific components Lsm11 and U7 snRNA, we rescued U7 snRNP levels and processing defects in SUMO2 knockout cells. Through analysis of Lsm11, we identified a SUMO-interacting motif in its N terminus required for efficient formation of U7 snRNP. Collectively, we demonstrated that SUMO2 promotes histone pre-mRNA 3′ end processing by stabilizing HLB interactions and facilitating U7 snRNP assembly.
科研通智能强力驱动
Strongly Powered by AbleSci AI