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马查多-约瑟夫病蛋白中扩展的聚谷氨酰胺在体外和体内均可诱导细胞死亡。

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo.

作者信息

Ikeda H, Yamaguchi M, Sugai S, Aze Y, Narumiya S, Kakizuka A

机构信息

Department of Pharmacology, Kyoto University Faculty of Medicine, Japan.

出版信息

Nat Genet. 1996 Jun;13(2):196-202. doi: 10.1038/ng0696-196.

Abstract

Recently, we identified a novel gene, MJD1, which contains an expanded CAG triplet repeat in Machado-Joseph disease. Here we report the induction of apoptosis in cultured cells expressing a portion of the MJD1 gene that includes the expanded CAG repeats. Cell death occurs only when the CAG repeat is translated into polyglutamine residues, which apparently precipitate in large covalently modified forms. We also created ataxic transgenic mice by expressing the expanded polyglutamine stretch in Purkinje cells. Our results demonstrate the potential involvement of the expanded polyglutamine as the common aetiological agent for inherited neurodegenerative diseases with CAG expansions.

摘要

最近,我们鉴定出一个新基因MJD1,它在马查多-约瑟夫病中含有一个扩增的CAG三联体重复序列。在此我们报告,在表达包含扩增CAG重复序列的部分MJD1基因的培养细胞中诱导了细胞凋亡。细胞死亡仅在CAG重复序列被翻译成聚谷氨酰胺残基时发生,这些聚谷氨酰胺残基显然以大的共价修饰形式沉淀。我们还通过在浦肯野细胞中表达扩增的聚谷氨酰胺片段创建了共济失调转基因小鼠。我们的结果表明,扩增的聚谷氨酰胺作为具有CAG扩增的遗传性神经退行性疾病的常见病因可能发挥作用。

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