PROLINE-DIRECTED AND NON-PROLINE-DIRECTED PHOSPHORYLATION OF PHF-TAU

被引:527
作者
MORISHIMAKAWASHIMA, M
HASEGAWA, M
TAKIO, K
SUZUKI, M
YOSHIDA, H
TITANI, K
IHARA, Y
机构
[1] UNIV TOKYO, FAC MED,INST BRAIN RES,DEPT NEUROPATHOL,BUNKYO KU, TOKYO 113, JAPAN
[2] RIKEN, INST PHYS & CHEM RES, DIV BIOMOLEC CHARACTERIZAT, WAKO, SAITAMA 35101, JAPAN
[3] RIKEN, INST PHYS & CHEM RES, BIODESIGN RES GRP, WAKO, SAITAMA 35101, JAPAN
[4] FUJITA HLTH UNIV, SCH MED, INST COMPREHENS MED SCI, DIV BIOMED POLYMER SCI, TOYOAKE, AICHI 47011, JAPAN
关键词
D O I
10.1074/jbc.270.2.823
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
To gain insight into the abnormal phosphorylation of PHF-tau, we have determined the phosphorylation sites by identifying phosphopeptides by means of ion spray mass spectrometry followed by sequencing of ethane-thiol-modified peptides. Nineteen sites have been identified; all but Ser-262 are localized to the amino- and carboxyl-terminal flanking regions of the microtubule binding domain, Eleven sites correspond to fetal type sites. Unexpectedly, 10 are non-proline-directed, whereas the others are proline-directed. Thus, the abnormal phosphorylation of PHF-tau can be considered to consist of fetal type phosphorylation and additional pro line-directed and non-proline directed phosphorylation. This non-fetal type phosphorylation may provide PHF-tau with the unusual characteristics.
引用
收藏
页码:823 / 829
页数:7
相关论文
共 72 条
[1]   ROLE OF ABNORMALLY PHOSPHORYLATED TAN IN THE BREAKDOWN OF MICROTUBULES IN ALZHEIMER-DISEASE [J].
ALONSO, AD ;
ZAIDI, T ;
GRUNDKEIQBAL, I ;
IQBAL, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5562-5566
[2]   TAU-PROTEIN KINASE-II IS INVOLVED IN THE REGULATION OF THE NORMAL PHOSPHORYLATION STATE OF TAU-PROTEIN [J].
ARIOKA, M ;
TSUKAMOTO, M ;
ISHIGURO, K ;
KATO, R ;
SATO, K ;
IMAHORI, K ;
UCHIDA, T .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (02) :461-468
[3]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[4]   CASEIN KINASE-II IS ASSOCIATED WITH NEUROFIBRILLARY TANGLES BUT IS NOT AN INTRINSIC COMPONENT OF PAIRED HELICAL FILAMENTS [J].
BAUM, L ;
MASLIAH, E ;
IIMOTO, DS ;
HANSEN, LA ;
HALLIDAY, WC ;
SAITOH, T .
BRAIN RESEARCH, 1992, 573 (01) :126-132
[5]   THE SWITCH OF TAU-PROTEIN TO AN ALZHEIMER-LIKE STATE INCLUDES THE PHOSPHORYLATION OF 2 SERINE PROLINE MOTIFS UPSTREAM OF THE MICROTUBULE BINDING REGION [J].
BIERNAT, J ;
MANDELKOW, EM ;
SCHROTER, C ;
LICHTENBERGKRAAG, B ;
STEINER, B ;
BERLING, B ;
MEYER, H ;
MERCKEN, M ;
VANDERMEEREN, A ;
GOEDERT, M ;
MANDELKOW, E .
EMBO JOURNAL, 1992, 11 (04) :1593-1597
[6]   PHOSPHORYLATION OF SER(262) STRONGLY REDUCES BINDING OF TAU-PROTEIN TO MICROTUBULES - DISTINCTION BETWEEN PHF-LIKE IMMUNOREACTIVITY AND MICROTUBULE-BINDING [J].
BIERNAT, J ;
GUSTKE, N ;
DREWES, G ;
MANDELKOW, EM ;
MANDELKOW, E .
NEURON, 1993, 11 (01) :153-163
[7]   TAU IN ALZHEIMER NEUROFIBRILLARY TANGLES - N-TERMINAL AND C-TERMINAL REGIONS ARE DIFFERENTIALLY ASSOCIATED WITH PAIRED HELICAL FILAMENTS AND THE LOCATION OF A PUTATIVE ABNORMAL PHOSPHORYLATION SITE [J].
BRION, JP ;
HANGER, DP ;
BRUCE, MT ;
COUCK, AM ;
FLAMENTDURAND, J ;
ANDERTON, BH .
BIOCHEMICAL JOURNAL, 1991, 273 :127-133
[8]   PURIFICATION OF TAU, A MICROTUBULE-ASSOCIATED PROTEIN THAT INDUCES ASSEMBLY OF MICROTUBULES FROM PURIFIED TUBULIN [J].
CLEVELAND, DW ;
HWO, SY ;
KIRSCHNER, MW .
JOURNAL OF MOLECULAR BIOLOGY, 1977, 116 (02) :207-225
[9]  
CORREAS I, 1992, J BIOL CHEM, V267, P15721
[10]   ASSEMBLY OF ALZHEIMER-LIKE FILAMENTS FROM FULL-LENGTH TAU-PROTEIN [J].
CROWTHER, RA ;
OLESEN, OF ;
SMITH, MJ ;
JAKES, R ;
GOEDERT, M .
FEBS LETTERS, 1994, 337 (02) :135-138