Investigating gene-to-behavior pathways in psychiatric disorders - The use of a comprehensive behavioral test battery on genetically engineered mice

被引:40
作者
Takao, Keizo [1 ]
Miyakawa, Tsuyoshi [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Horizontal Med Res Org, Kyoto 6068501, Japan
来源
INTEGRATED MOLECULAR MEDICINE FOR NEURONAL AND NEOPLASTIC DISORDERS | 2006年 / 1086卷
关键词
comprehensive behavioral test battery; psychiatric diseases; genetically engineered mice; animal model of schizophrenia; calcineurin;
D O I
10.1196/annals.1377.008
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
We have been investigating the relationships between genes and behaviors by conducting a systematic and well-defined behavioral test battery with mice that have a mutation on a gene of interest. The behavioral test battery covers a relatively broad range of various behavioral domains such as learning and memory, sensory-motor functions, emotion, motivation, and drug sensitivity/preference. Recently, we subjected mice lacking calcineurin (CN), a calcium/calmodulin protein phosphatase, to the comprehensive behavioral test battery. The mutant mice had a severe working memory deficit, increased locomotor activity, decreased social interaction, and impairments in prepulse and latent inhibition. The abnormalities of CN mutant mice were strikingly similar to those described for schizophrenic patients. Consistent with these findings, human genetics studies in a large sample of affected families detected a significant association of the PPP3CC gene, which encodes the CN gamma catalytic subunit with schizophrenia. The idea that abnormalities in the CN signaling pathway are involved in schizophrenia pathogenesis is consistent with traditional theories of schizophrenia and with many facts known about schizophrenia. A tremendous amount of knowledge about CN has accumulated and, by utilizing this information, the studies on the pathogenesis/pathophysiology of schizophrenia and its related mental disorders will be potentially accelerated. We discuss the potential impact of a large-scale mouse phenotyping project on the study of psychiatric disorders.
引用
收藏
页码:144 / 159
页数:16
相关论文
共 78 条
[11]   SPATIAL MEMORY AND N-METHYL-D-ASPARTATE RECEPTOR ANTAGONISTS APV AND MK-801 - MEMORY IMPAIRMENTS DEPEND ON FAMILIARITY WITH THE ENVIRONMENT, DRUG DOSE, AND TRAINING DURATION [J].
CARAMANOS, Z ;
SHAPIRO, ML .
BEHAVIORAL NEUROSCIENCE, 1994, 108 (01) :30-43
[12]   Fimbria-fornix vs selective hippocampal lesions in rats: Effects on locomotor activity and spatial learning and memory [J].
Cassel, JC ;
Cassel, S ;
Galani, R ;
Kelche, C ;
Will, B ;
Jarrard, L .
NEUROBIOLOGY OF LEARNING AND MEMORY, 1998, 69 (01) :22-45
[13]   ASYMMETRIC RETRACTION OF GROWTH CONE FILOPODIA FOLLOWING FOCAL INACTIVATION OF CALCINEURIN [J].
CHANG, HY ;
TAKEI, K ;
SYDOR, AM ;
BORN, T ;
RUSNAK, F ;
JAY, DG .
NATURE, 1995, 376 (6542) :686-690
[14]   Evidence for a chromosome 2p13-14 schizophrenia susceptibility locus in families from Palau, Micronesia [J].
Coon, H ;
Myles-Worsley, M ;
Tiobech, J ;
Hoff, M ;
Rosenthal, J ;
Bennett, P ;
Reimherr, F ;
Wender, P ;
Dale, P ;
Polloi, A ;
Byerley, W .
MOLECULAR PSYCHIATRY, 1998, 3 (06) :521-527
[15]   The dephosphins: dephosphorylation by calcineurin triggers synaptic vesicle endocytosis [J].
Cousin, MA ;
Robinson, PJ .
TRENDS IN NEUROSCIENCES, 2001, 24 (11) :659-665
[16]   Calcium, calcineurin, and the control of transcription [J].
Crabtree, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (04) :2313-2316
[17]   Generic signals and specific outcomes:: Signaling through Ca2+, calcineurin, and NF-AT [J].
Crabtree, GR .
CELL, 1999, 96 (05) :611-614
[18]   CYCLOSPORINE-ASSOCIATED ORGANIC MENTAL-DISORDERS IN LIVER-TRANSPLANT RECIPIENTS [J].
CRAVEN, JL .
PSYCHOSOMATICS, 1991, 32 (01) :94-102
[19]   Designing mouse behavioral tasks relevant to autistic-like behaviors [J].
Crawley, JN .
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2004, 10 (04) :248-258
[20]  
CRAWLEY JN, 2000, WRONG WITH MY MOUSE