DISC1 localizes to the centrosome by binding to kendrin

被引:89
作者
Miyoshi, K
Asanuma, M
Miyazaki, I
Diaz-Corrales, FJ
Katayama, T
Tohyama, M
Ogawa, N
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Brain Sci, Okayama 7008558, Japan
[2] Osaka Univ, Grad Sch Med, Dept Anat & Neurosci, Suita, Osaka 5650871, Japan
关键词
DISC1; kendrin; pericentrin; centrosome; mental disorders; schizophrenia; affective disorders;
D O I
10.1016/j.bbrc.2004.03.163
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
Disrupted-In-Schizophrenia 1 (DISC1) was identified as a novel gene disrupted by a (1; 11)(q42.1;q 14.3) translocation that segregated with major mental disorders in a Scottish family. Using the yeast two-hybrid system, we screened a human brain cDNA library for interactors of the DISC1 protein. One of the positive clones encoded kendrin/pericentrin-B, a giant protein known to localize specifically to the centrosome. The interaction between DISCI and kendrin in mammalian cells was demonstrated by an immunoprecipitation assay. Residues 446-533 of DISC1 were essential for the interaction with kendrin. Immunocytochemical analysis revealed the colocalization of DISC1 and kendrin to the centrosome. These data indicate that DISC1 localizes to the centrosome by binding to kendrin. Kendrin has been reported to anchor the gamma-tubulin complex to the centrosome, providing microtubule nucleation sites. The present study suggests the possible involvement of DISC1 in the pathophysiology of mental disorders due to its putative effect on centrosomal function. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1195 / 1199
页数:5
相关论文
共 28 条
[1]   Manic-depression genes and the new millennium: poised for discovery [J].
Baron, M .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :342-358
[2]   Schizophrenia and affective disorders - Cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: Clinical and P300 findings in a family [J].
Blackwood, DHR ;
Fordyce, A ;
Walker, MT ;
St Clair, DM ;
Porteous, DJ ;
Muir, WJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (02) :428-433
[3]   Chromosome 1 loci in Finnish schizophrenia families [J].
Ekelund, J ;
Hovatta, I ;
Parker, A ;
Paunio, T ;
Varilo, T ;
Martin, R ;
Suhonen, J ;
Ellonen, P ;
Chan, GY ;
Sinsheimer, JS ;
Sobel, E ;
Juvonen, H ;
Arajärvi, R ;
Partonen, T ;
Suvisaari, J ;
Lönnqvist, J ;
Meyer, J ;
Peltonen, L .
HUMAN MOLECULAR GENETICS, 2001, 10 (15) :1611-1617
[4]   Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin [J].
Flory, MR ;
Moser, MJ ;
Monnat, RJ ;
Davis, TN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :5919-5923
[5]   THE ESSENTIAL MITOTIC TARGET OF CALMODULIN IS THE 110-KILODALTON COMPONENT OF THE SPINDLE POLE BODY IN SACCHAROMYCES-CEREVISIAE [J].
GEISER, JR ;
SUNDBERG, HA ;
CHANG, BH ;
MULLER, EGD ;
DAVIS, TN .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) :7913-7924
[6]  
Gillingham AK, 2000, EMBO REP, V1, P524
[7]   The neuropathology of schizophrenia - A critical review of the data and their interpretation [J].
Harrison, PJ .
BRAIN, 1999, 122 :593-624
[8]   Neuropathological studies of synaptic connectivity in the hippocampal formation in schizophrenia [J].
Harrison, PJ ;
Eastwood, SL .
HIPPOCAMPUS, 2001, 11 (05) :508-519
[9]   Hippocampal neurons in schizophrenia [J].
Heckers, S ;
Konradi, C .
JOURNAL OF NEURAL TRANSMISSION, 2002, 109 (5-6) :891-905
[10]   Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects [J].
Hennah, W ;
Varilo, T ;
Kestilä, M ;
Paunio, T ;
Arajärvi, R ;
Haukka, J ;
Parker, A ;
Martin, R ;
Levitzky, S ;
Partonen, T ;
Meyer, J ;
Lönnqvist, J ;
Peltonen, L ;
Ekelund, J .
HUMAN MOLECULAR GENETICS, 2003, 12 (23) :3151-3159