Interaction between mutant ataxin-1 and POBP-1 affects transcription and cell death

被引:162
作者
Okazawa, H
Rich, T
Chang, A
Lin, X
Waragai, M
Kajikawa, M
Enokido, Y
Komuro, A
Kato, S
Shibata, M
Hatanaka, H
Mouradian, MM
Sudol, M
Kanazawa, I
机构
[1] Univ Tokyo, Grad Sch med, Dept Neurol, Bunkyo Ku, Tokyo 1138655, Japan
[2] MBL Co Ltd, Dept Pharmaceut Dev, Nagano 3960002, Japan
[3] Osaka Univ, Inst Prot Res, Div Prot Biosynth, Suita, Osaka 5650871, Japan
[4] JST, ERATO, Sagami Chem Res Ctr, Kanagawa 2290012, Japan
[5] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[6] Mt Sinai Med Ctr, Dept Med, New York, NY 10029 USA
[7] Baylor Coll Med, Howard Hughes Med Inst, Dept Pediat Neurol Neurosci & Mol Genet, Houston, TX 77030 USA
[8] NINCDS, Expt Therapeut Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0896-6273(02)00697-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
PQBP-1 was isolated on the basis of its interaction with polyglutamine tracts. In this study, using in vitro and in vivo assays, we show that the association between ataxin-1 and PQBP-1 is positively influenced by expanded polyglutamine sequences. In cell lines, interaction between the two molecules induces apoptotic cell death. As a possible mechanism underlying this phenomenon, we found that mutant ataxin-1 enhances binding of PQBP-1 to the C-terminal domain of RNA polymerase II large subunit (Pol II). This reduces the level of phosphorylated Pol II and transcription. Our results suggest the involvement of PQBP-1 in the pathology of spinocerebellar ataxia type 1 (SCA1) and support the idea that modified transcription underlies polyglutamine-mediated pathology.
引用
收藏
页码:701 / 713
页数:13
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