Modeling human neurodegenerative diseases in transgenic systems

被引:81
作者
Sosa, Miguel A. Gama [1 ,2 ,3 ]
De Gasperi, Rita [1 ,2 ,3 ]
Elder, Gregory A. [2 ,3 ,4 ,5 ]
机构
[1] Vet Affairs Med Ctr, James J Peters Dept, Res & Dev Serv, Bronx, NY 10468 USA
[2] NYU, Dept Psychiat, Mt Sinai Sch Med, New York, NY 10016 USA
[3] NYU, Mt Sinai Sch Med, Friedman Brain Inst, New York, NY USA
[4] Vet Affairs Med Ctr, James J Peters Dept, Neurol Serv, Bronx, NY 10468 USA
[5] NYU, Dept Neurol, Mt Sinai Sch Med, New York, NY 10016 USA
关键词
SITE-SPECIFIC RECOMBINATION; AMYLOID PRECURSOR PROTEIN; CAENORHABDITIS-ELEGANS MODEL; CONDITIONAL GENE-EXPRESSION; CRE-MEDIATED RECOMBINATION; MOTOR-NEURON DEGENERATION; INTRANEURONAL-A-BETA; ALZHEIMERS-DISEASE; HUNTINGTONS-DISEASE; MOUSE MODEL;
D O I
10.1007/s00439-011-1119-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Transgenic systems are widely used to study the cellular and molecular basis of human neurodegenerative diseases. A wide variety of model organisms have been utilized, including bacteria (Escherichia coli), plants (Arabidopsis thaliana), nematodes (Caenorhabditis elegans), arthropods (Drosophila melanogaster), fish (zebrafish, Danio rerio), rodents (mouse, Mus musculus and rat, Rattus norvegicus) as well as non-human primates (rhesus monkey, Macaca mulatta). These transgenic systems have enormous value for understanding the pathophysiological basis of these disorders and have, in some cases, been instrumental in the development of therapeutic approaches to treat these conditions. In this review, we discuss the most commonly used model organisms and the methodologies available for the preparation of transgenic organisms. Moreover, we provide selected examples of the use of these technologies for the preparation of transgenic animal models of neurodegenerative diseases, including Alzheimer's disease (AD), frontotemporal lobar degeneration (FTLD), amyotrophic lateral sclerosis (ALS), Huntington's disease (HD) and Parkinson's disease (PD) and discuss the application of these technologies to AD as an example of how transgenic modeling has affected the study of human neurodegenerative diseases.
引用
收藏
页码:535 / 563
页数:29
相关论文
共 329 条
[51]   The lac operator-repressor system is functional in the mouse [J].
Cronin, CA ;
Gluba, W ;
Scrable, H .
GENES & DEVELOPMENT, 2001, 15 (12) :1506-1517
[52]   Intraneuronal Aβ, non-amyloid aggregates and neurodegeneration in a Drosophila model of Alzheimer's disease [J].
Crowther, DC ;
Kinghorn, KJ ;
Miranda, E ;
Page, R ;
Curry, JA ;
Duthie, FAI ;
Gubb, DC ;
Lomas, DA .
NEUROSCIENCE, 2005, 132 (01) :123-135
[53]   Targeted integration in rat and mouse embryos with zinc- finger nucleases [J].
Cui, Xiaoxia ;
Ji, Diana ;
Fisher, Daniel A. ;
Wu, Yumei ;
Briner, David M. ;
Weinstein, Edward J. .
NATURE BIOTECHNOLOGY, 2011, 29 (01) :64-+
[54]   Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation [J].
Davies, SW ;
Turmaine, M ;
Cozens, BA ;
DiFiglia, M ;
Sharp, AH ;
Ross, CA ;
Scherzinger, E ;
Wanker, EE ;
Mangiarini, L ;
Bates, GP .
CELL, 1997, 90 (03) :537-548
[55]   Gene activation using FLP recombinase in C-elegans [J].
Davis, M. Wayne ;
Morton, J. Jason ;
Carroll, Dana ;
Jorgensen, Erik M. .
PLOS GENETICS, 2008, 4 (03)
[56]   The IRG mouse: A two-color fluorescent reporter for assessing Cre-mediated recombination and imaging complex cellular relationships in situ [J].
De Gasperi, Rita ;
Rocher, Anne B. ;
Sosa, Miguel A. Gama ;
Wearne, Susan L. ;
Perez, Gissel M. ;
Friedrich, Victor L., Jr. ;
Hof, Patrick R. ;
Elder, Gregory A. .
GENESIS, 2008, 46 (06) :308-317
[57]   Conditional Transgene and Gene Targeting Methodologies in Zebrafish [J].
Deiters, Alexander ;
Yoder, Jeffrey A. .
ZEBRAFISH, 2006, 3 (04) :415-429
[58]  
DEUSCHLE U, 1995, MOL CELL BIOL, V15, P1907
[59]   Optimized Gal4 genetics for permanent gene expression mapping in zebrafish [J].
Distel, Martin ;
Wullimann, Mario F. ;
Koester, Reinhard W. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (32) :13365-13370
[60]   Caenorhabditis elegans reporter fusion genes generated by seamless modification of large genomic DNA clones [J].
Dolphin, Colin T. ;
Hope, Ian A. .
NUCLEIC ACIDS RESEARCH, 2006, 34 (09)