Large-scale identification of differentially expressed genes during neurogenesis

被引:4
作者
Pazman, C
Castelli, JC
Wen, XL
Somogyi, R
机构
[1] NINDS, Neurophysiol Lab, Bethesda, MD 20892 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
关键词
differential display; NGF; PC12; spinal cord;
D O I
10.1097/00001756-200003200-00013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We report here a modified mRNA differential display method and its application for the analysis of differential gene expression in NGF-treated PC12 cells and in embryonic rat spinal cord. The optimized protocol is based on low fidelity priming of multiple cDNAs followed by high fidelity amplification. In PC12 cells induction by nerve growth factor (NGF) altered the expression of 4% of the 466 transcripts evaluated. During neurogenesis of the spinal cord we found that 30% of the 288 examined products changed. The differential expression of the characterized genes was confirmed by independent quantitative PCR. We conclude this method is suitable for the identification of increases and decreases of mRNA levels and allows the discovery of differentially expressed unknown transcripts. NeuroReport 11:719-724 (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:719 / 724
页数:6
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