Chen Z J, Shen H, Tew K D
Department of Pharmacology, Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, PA 19111, USA.
Nucleic Acids Res. 2001 May 15;29(10):E46. doi: 10.1093/nar/29.10.e46.
Amplified differential gene expression (ADGE) is a novel technique, designed to profile gene expression of the whole transcriptome or to compare expression of a set of genes between two samples. ADGE employs hybridization to quadratically amplify the ratio of an expressed gene between control and tester samples before displaying. The subtle structures of adapters and primers are designed for displaying the amplified ratio of an expressed gene between two samples. Four selective nucleotides at the 3' end of primers are used to increase PCR efficiency for targeted molecules and to improve detection of PCR products. Double PCR with the same pair of primers expands the detection range, especially for genes of low abundance. Integration of these steps makes ADGE sensitive and accurate. Application to drug resistant human tumor cell lines showed that ADGE accurately profiled expression levels for induced, repressed or unchanged genes. The qualitative expression patterns for ADGE were verified with RT-PCR.
扩增差异基因表达(ADGE)是一种新技术,旨在分析整个转录组的基因表达情况,或比较两个样本之间一组基因的表达。ADGE采用杂交技术,在展示之前对对照样本和测试样本中表达基因的比例进行二次扩增。衔接子和引物的精细结构设计用于展示两个样本之间表达基因的扩增比例。引物3'端的四个选择性核苷酸用于提高靶向分子的PCR效率,并改善PCR产物的检测。使用同一对引物进行双重PCR可扩大检测范围,尤其是对于低丰度基因。这些步骤的整合使ADGE灵敏且准确。应用于耐药性人类肿瘤细胞系表明,ADGE能准确分析诱导、抑制或未改变基因的表达水平。ADGE的定性表达模式通过RT-PCR得到验证。