Iacobas Andrei D, Urban Marcia, Massimi Aldo, Spray David C
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
J Biomol Tech. 2002 Mar;13(1):5-19.
We studied six types of errors that affect the experimental results obtained with the spotted cDNA technology, proposing a new experimental strategy and a four-step algorithm to improve data accuracy. In an experiment analyzed with this method, mRNA extracted from neuroblastoma (N2A) cells and a clone transfected with the neuronal gap junction protein Cx36 were hybridized on 10 chips, each spotted with 2512 known mouse cDNAs. We found 53 upregulated and 23 downregulated genes with expression ratios exceeding 1.5-fold. By contrast, the newly introduced standard gene expression score, which considers the normal variability of gene expression in the reference cells, revealed that Cx36 transfection (p < 0.05) upregulated 161 genes and downregulated 61 genes. These results demonstrate the necessity to correct the raw data obtained from cDNA microarrays for systematic errors and indicate that use of the standard expression score significantly extends the identification of gene expression changes following experimental intervention.
我们研究了影响斑点cDNA技术所获实验结果的六种误差类型,提出了一种新的实验策略和一个四步算法以提高数据准确性。在用该方法分析的一项实验中,从神经母细胞瘤(N2A)细胞提取的mRNA以及转染了神经元间隙连接蛋白Cx36的一个克隆,在10个芯片上进行杂交,每个芯片上点有2512个已知的小鼠cDNA。我们发现表达率超过1.5倍的上调基因有53个,下调基因有23个。相比之下,新引入的标准基因表达评分考虑了参考细胞中基因表达的正常变异性,结果显示Cx36转染(p < 0.05)使161个基因上调,61个基因下调。这些结果证明了校正从cDNA微阵列获得的原始数据以消除系统误差的必要性,并表明使用标准表达评分能显著扩展对实验干预后基因表达变化的识别。