Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation

被引:180
作者
Dayanandan, R
Van Slegtenhorst, M
Mack, TGA
Ko, L
Yen, SH
Leroy, K
Brion, JP
Anderton, BH
Hutton, M
Lovestone, S
机构
[1] Inst Psychiat, Dept Neurosci, London SE5 8AF, England
[2] Inst Psychiat, Dept Old Age Psychiat, London SE5 8AF, England
[3] Mayo Clin Jacksonville, Jacksonville, FL 32224 USA
[4] Free Univ Brussels, Lab Pathol & Electron Microscopy, B-1070 Brussels, Belgium
基金
英国惠康基金;
关键词
tau; fronto-temporal degeneration; mutation; microtubule; GSK-3;
D O I
10.1016/S0014-5793(99)00222-7
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
In vitro evidence has suggested a change in the ability of tau bearing mutations associated with fronto-temporal dementia to promote microtubule assembly. We have used a cellular assay to quantitate the effect of both isoform differences and mutations on the physiological function of tau, Whilst all variants of tan bind to microtubules, microtubule extension is reduced in cells transfected with 3-relative to 4-repeat tau, Mutations reduce microtubule extension with the P301L mutation having a greater effect than the V337M mutation. The R406W mutation had a small effect on microtubule extension but, surprisingly, tau with this mutation was less phosphorylated in intact cells than the other variants. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:228 / 232
页数:5
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