A genetic analysis of neural progenitor differentiation

被引:199
作者
Geschwind, DH [1 ]
Ou, J
Easterday, MC
Dougherty, JD
Jackson, RL
Chen, ZG
Antoine, H
Terskikh, A
Weissman, IL
Nelson, SF
Kornblum, HI
机构
[1] Univ Calif Los Angeles, Sch Med, Neurogenet Program, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Pediat, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Crump Inst Mol Imaging, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, Sch Med, Mental Retardat Res Ctr, Los Angeles, CA 90095 USA
[8] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[9] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
关键词
D O I
10.1016/S0896-6273(01)00209-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Genetic mechanisms regulating CNS progenitor function and differentiation are not well understood. We have used microarrays derived from a representational difference analysis (RDA) subtraction in a heterogeneous stem cell culture system to systematically study the gene expression patterns of CNS progenitors. This analysis identified both known and novel genes enriched in progenitor cultures. In situ hybridization in a subset of clones demonstrated that many of these genes were expressed preferentially in germinal zones, some showing distinct ventricular or subventricular zone labeling. Several genes were also enriched in hematopoietic stem cells, suggesting an overlap of gene expression in neural and hematopoietic progenitors. This combination of methods demonstrates the power of using custom microarrays derived from RDA-subtracted libraries for both gene discovery and gene expression analysis in the central nervous system.
引用
收藏
页码:325 / 339
页数:15
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