The C-Terminus of Tau Protein Plays an Important Role in Its Stability and Toxicity

被引:10
|
作者
Geng, Junhua [1 ,2 ,3 ]
Xia, Lu [1 ,2 ,3 ]
Li, Wanjie [1 ,2 ,3 ]
Dou, Fei [1 ,2 ,3 ,4 ]
机构
[1] Beijing Normal Univ, State Key Lab Cognit Neurosci & Learning, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, IDG McGovern Inst Brain Res, Beijing 100875, Peoples R China
[3] Beijing Normal Univ, Ctr Collaborat & Innovat Brain & Learning Sci, Beijing 100875, Peoples R China
[4] Beijing Normal Univ, Coll Life Sci, Beijing 100875, Peoples R China
基金
中国国家自然科学基金;
关键词
Tauopathies; Protein degradation; Proteolysis; Drosophila; MICROTUBULE-ASSOCIATED PROTEIN; NEUROFIBRILLARY TANGLES; CASPASE CLEAVAGE; CATHEPSIN-D; MUTATION; TAUOPATHY; DEMENTIA; SUPPRESSION; PROTEOLYSIS; GENE;
D O I
10.1007/s12031-014-0314-7
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
The identification of tau fragments generated by proteolysis in the neurons of AD patients and in neurofibrillary tangles encourages research on the toxicity of truncated tau. However, the detailed mechanism underlying the proteolysis-induced toxicity of tau is not clear and even controversial in some cases. In the present study, we used Drosophila as a model to evaluate the toxicity of a set of truncated tau fragments in vivo and found that the flies harboring C-terminal-truncated tau exhibited less toxicity due to the unstable characteristic of C-terminal-truncated tau fragments. Further study carried out in cultured Drosophila Kc cells revealed that C-terminal-truncated tau fragments degrade faster than full-length tau or N-terminal-truncated fragments. Collectively, our data implicate proteolysis of tau as an important pathway mediating tau degradation and neurotoxicity in vivo.
引用
收藏
页码:251 / 259
页数:9
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