Duplàa C, Couffinhal T, Labat L, Moreau C, Lamazière J M, Bonnet J
Inserm Unité 8 de Cardiologie, Pessac, France.
Anal Biochem. 1993 Jul;212(1):229-36. doi: 10.1006/abio.1993.1316.
A method for relative quantitation of specific mRNA species by polymerase chain reaction (PCR) has been developed by using the incorporation of biotinylated dUTP. Transferred biotinylated PCR products gave a sensitive colorimetric signal which could be quantitated by video analysis. In the exponential phase of amplification, the linearity and reproducibility of reverse transcription and PCR demonstrated the same efficiency of cDNA synthesis and PCR for the two target genes, ICAM-1 and beta-actin, and allowed the normalization of ICAM-1 expression. These results suggested that in the exponential phase of amplification a relative quantitation of mRNA could be determined. We used this approach to analyze the different effects of TNF-alpha, IL-1 beta, and purified porcine platelet-derived growth factor stimulations on ICAM-1 expression in smooth muscle cells.
通过掺入生物素化的dUTP,开发了一种利用聚合酶链反应(PCR)对特定mRNA种类进行相对定量的方法。转移的生物素化PCR产物产生了灵敏的比色信号,可通过视频分析进行定量。在扩增的指数期,逆转录和PCR的线性和可重复性表明,针对两个靶基因ICAM-1和β-肌动蛋白,cDNA合成和PCR的效率相同,并且可以对ICAM-1表达进行标准化。这些结果表明,在扩增的指数期,可以确定mRNA的相对定量。我们使用这种方法来分析肿瘤坏死因子-α、白细胞介素-1β和纯化的猪血小板衍生生长因子刺激对平滑肌细胞中ICAM-1表达的不同影响。