snRNP公司
小核RNA
剪接体
RNA剪接
卡哈尔体
核糖核酸
核糖核蛋白
细胞质
Prp24型
生物
化学
细胞核
细胞生物学
分子生物学
生物化学
非编码RNA
基因
作者
Chadwick M. Hales,Eric B. Dammer,Ian Diner,Hong Yi,Nicholas T. Seyfried,Marla Gearing,Jonathan D. Glass,Thomas J. Montine,Allan I. Levey,James J. Lah
摘要
Abstract We recently discovered that protein components of the ribonucleic acid ( RNA ) spliceosome form cytoplasmic aggregates in A lzheimer's disease ( AD ) brain, resulting in widespread changes in RNA splicing. However, the involvement of small nuclear RNAs ( snRNAs ), also key components of the spliceosome complex, in the pathology of AD remains unknown. Using immunohistochemical staining of post‐mortem human brain and spinal cord, we identified cytoplasmic tangle‐shaped aggregates of snRNA in both sporadic and familial AD cases but not in aged controls or other neurodegenerative disorders. Immunofluorescence using antibodies reactive with the 2,2,7‐trimethylguanosine cap of snRNAs and transmission electron microscopy demonstrated snRNA localization with tau and paired helical filaments, the main component of neurofibrillary tangles. Quantitative real‐time polymerase chain reaction ( PCR ) showed U 1 snRNA accumulation in the insoluble fraction of AD brains whereas other U snRNAs were not enriched. In combination with our previous results, these findings demonstrate that aggregates of U 1 snRNA and U 1 small nuclear ribonucleoproteins represent a new pathological hallmark of AD .
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