Different complex formations of dentatorubral-pallidoluysian atrophy (DRPLA) protein in human and rat neurons

被引:5
|
作者
Yazawa, I
Hazeki, N
Kanazawa, I
机构
[1] Toranomon Hosp, Dept Neurol, Minato Ku, Tokyo 1058470, Japan
[2] Okinaka Mem Inst Med Res, Minato Ku, Tokyo 1058470, Japan
[3] Univ Tokyo, Grad Sch Med, Div Neurosci, Dept Neurol,Bunkyo Ku, Tokyo 1138655, Japan
关键词
D O I
10.1006/bbrc.1998.9640
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dentatorubral-pallidoluysian atrophy (DRPLA) is caused by expansion of a glutamine repeat in DRPLA protein. Rat DRPLA protein, homologous in sequence to human DRPLA protein, was identified in rat brains. Immunoblots of human control and rat brain tissues with and without reduction show that human DRPLA protein forms more disulfide-bond complexes than rat DRPLA protein. An immunohistochemical study and a subcellular fractionation experiment show that human DRPLA protein produces complexes within the cytoplasm of neurons, whereas rat DRPLA protein rarely does. In spite of the close homology of their amino acid sequences, human and rat DRPLA protein have different protein characters. The differences in these characters suggest structural differences and may be related to these proteins functions. (C) 1998 Academic Press.
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页码:209 / 213
页数:5
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