Mouse Genetic Models of Human Brain Disorders

被引:34
|
作者
Leung, Celeste [1 ,2 ]
Jia, Zhengping [1 ,2 ]
机构
[1] Hosp Sick Children, Program Neurosci & Mental Hlth, Peter Organ Ctr Res & Learning, 555 Univ Ave, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Program Physiol, Toronto, ON, Canada
关键词
genetic models; transgenic mice; gene targeting; knockout; knock-in; inducible; brain disorders; behavior; FRAGILE-X-SYNDROME; AMYLOID PRECURSOR PROTEIN; FAMILIAL ALZHEIMERS-DISEASE; LINKED MENTAL-RETARDATION; EARLY-ONSET PARKINSONISM; WILLIAMS-BEUREN SYNDROME; COMMON LRRK2 MUTATION; KNOCKOUT MICE REVEAL; TAU-DEFICIENT MICE; DISC1 MUTANT MICE;
D O I
10.3389/fgene.2016.00040
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Over the past three decades, genetic manipulations in mice have been used in neuroscience as a major approach to investigate the in vivo function of genes and their alterations. In particular, gene targeting techniques using embryonic stem cells have revolutionized the field of mammalian genetics and have been at the forefront in the generation of numerous mouse models of human brain disorders. In this review, we will first examine childhood developmental disorders such as autism, intellectual disability, Fragile X syndrome, and Williams-Beuren syndrome. We will then explore psychiatric disorders such as schizophrenia and lastly, neurodegenerative disorders including Alzheimer's disease and Parkinson's disease. We will outline the creation of these mouse models that range from single gene deletions, subtle point mutations to multi-gene manipulations, and discuss the key behavioral phenotypes of these mice. Ultimately, the analysis of the models outlined in this review will enhance our understanding of the in vivo role and underlying mechanisms of disease-related genes in both normal brain function and brain disorders, and provide potential therapeutic targets and strategies to prevent and treat these diseases.
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页数:20
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