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Assessing the Expression of Two Genes Simultaneously in Surgical Specimens Using Polymerase Chain Reaction

机译:利用聚合酶链反应评估两个基因同时在手术标本中的表达

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We developed a novel polymerase chain reaction (PCR)-based method to analyze simultaneously the relative expression of two genes in a single PCR reaction. The method, relational PCR (R-PCR), utilizes special PCR primers that enable a PCR reaction to be converted from a standard uniplex reaction to a multiplex reaction in which all products are dependent on the same reaction components for amplification. We show that the quantitative ability of R-PCR is unaffected by sample nucleic acid input concentration over a range of 25-fold (30 to 750 ng of total RNA) and demonstrate excellent interexperimental reproducibility. We used R-PCR to analyze estrogen receptor gene expression in a series of invasive breast carcinomas, and our results show an excellent correlation between estrogen receptor mRNA expression and protein product accumulation determined by standard immunocytochemistry on paraffin sections.
机译:我们开发了一种新颖的基于聚合酶链反应(PCR)的方法,可以同时分析单个PCR反应中两个基因的相对表达。关系PCR(R-PCR)方法利用特殊的PCR引物,这些引物可使PCR反应从标准单重反应转化为多重反应,其中所有产物均依赖于相同的反应组分进行扩增。我们显示R-PCR的定量能力不受样品核酸输入浓度在25倍范围内(总RNA的30至750 ng)的影响,并显示出极好的实验间可重复性。我们使用R-PCR分析了一系列浸润性乳腺癌中雌激素受体基因的表达,我们的结果表明,通过石蜡切片上的标准免疫细胞化学测定,雌激素受体mRNA表达与蛋白积聚之间存在极好的相关性。

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