Large-scale genomic approaches to brain development and circuitry

被引:26
作者
Hatten, ME
Heintz, N
机构
[1] Rockefeller Univ, Dev Neurobiol Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Howard Hughes Med Inst, Mol Biol Lab, New York, NY 10021 USA
关键词
spontaneous mutant mice; ENU mutagenesis; gene trap vectors; BAC transgenic expression vectors; screens for novel CNS phenotypes and genotypes;
D O I
10.1146/annurev.neuro.26.041002.131436
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Over the past two decades, molecular genetic studies have enabled a common conceptual framework for the development and basic function of the nervous system. These studies, and the pioneering efforts of mouse geneticists and neuroscientists to identify and clone genes for spontaneous mouse mutants, have provided a paradigm for understanding complex processes of the vertebrate brain. Gene cloning for human brain malformations and degenerative disorders identified other important central nervous system (CNS) genes. However, because many debilitating human disorders are genetically complex, phenotypic screens are difficult to design. This difficulty has led to large-scale, genomic approaches to discover genes that are uniquely expressed in brain circuits and regions that control complex behaviors. In this review, we summarize current phenotype- and genotype-driven approaches to discover novel CNS-expressed genes, as well as current approaches to carry out large-scale, gene-expression screens in the CNS.
引用
收藏
页码:89 / 108
页数:20
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