Disrupted-in-schizophrenia-1 (DISC-1): Mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

被引:315
作者
Ozeki, Y
Tomoda, T
Kleiderlein, J
Kamiya, A
Bord, L
Fujii, K
Okawa, M
Yamada, N
Hatten, ME
Snyder, SH
Ross, CA
Sawa, A
机构
[1] Johns Hopkins Univ, Sch Med, Div Neurobiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[5] Shiga Univ Med Sci, Dept Psychiat, Otsu, Shiga 5202192, Japan
[6] Rockefeller Univ, Dev Neurobiol Lab, New York, NY 10021 USA
关键词
D O I
10.1073/pnas.0136913100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Disrupted-in-Schizophrenia-1 (DISC-1) is a gene whose mutant truncation is associated with major psychiatric illness with a predominance of schizophrenic symptomatology. We have cloned and characterized rodent DISC-1. DISC-1 expression displays pronounced developmental regulation with the highest levels in late embryonic life when the cerebral cortex develops. In yeast two-hybrid analyses, DISC-1 interacts with a variety of cytoskeletal proteins. One of these, NudE-like (NUDEL), is associated with cortical development and is linked to LIS-11, the disease gene for a form of lissencephaly, a disorder of cortical development. The disease mutant form of DISC-11 fails to bind NUDEL. Expression of mutant, but not wild-type, DISC-11 in PC12 cells reduces neurite extension. As schizophrenia is thought to reflect defects in cortical development that are determined by cytoskeletal protein activities, the cellular disturbances we observe with mutant DISC-11 may be relevant to psychopathologic mechanisms.
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页码:289 / 294
页数:6
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