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cDNA微阵列的技术分析

Technical analysis of cDNA microarrays.

作者信息

Scott Cinda P, VanWye Jeff, McDonald M Danielle, Crawford Douglas L

机构信息

Department of Marine Biology and Fisheries, Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, Florida, United States of America.

出版信息

PLoS One. 2009;4(2):e4486. doi: 10.1371/journal.pone.0004486. Epub 2009 Feb 16.

Abstract

BACKGROUND

There is extensive variation in gene expression among individuals within and between populations. Accurate measures of the variation in mRNA expression using microarrays can be confounded by technical variation, which includes variation in RNA isolation procedures, day of hybridization and methods used to amplify and dye label RNA for hybridization.

METHODOLOGY/PRINCIPAL FINDINGS: In this manuscript we analyze the relationship between the amount of mRNA and the fluorescent signal from the microarray hybridizations demonstrating that for a wide-range of mRNA concentrations the fluorescent signal is a linear function of the amount of mRNA. Additionally, the separate isolation, labeling or hybridization of RNA does not add significant amounts of variation in microarray measures of gene expression. However, single or double rounds of amplification for labeling do have small but significant affects on 10% of genes, but this source of technical variation is easy to avoid. To examine both technical and stochastic biological variation, mRNA expression was measured from the same five individuals over a six-week time course.

CONCLUSION

There were few, if any, meaningful differences in gene expression among time points. Thus, microarray measures using standard laboratory procedures can be precise and quantitative and are not subject to significant random biological noise.

摘要

背景

在群体内部以及群体之间,个体的基因表达存在广泛差异。使用微阵列准确测量mRNA表达的变异可能会受到技术变异的干扰,技术变异包括RNA分离程序、杂交日期以及用于扩增和对RNA进行染料标记以用于杂交的方法的变异。

方法/主要发现:在本论文中,我们分析了mRNA量与微阵列杂交荧光信号之间的关系,结果表明,对于广泛的mRNA浓度范围,荧光信号是mRNA量的线性函数。此外,RNA的单独分离、标记或杂交不会在基因表达的微阵列测量中增加显著的变异量。然而,单轮或两轮用于标记的扩增对10%的基因确实有微小但显著的影响,但这种技术变异来源很容易避免。为了研究技术变异和随机生物学变异,在六周的时间过程中对相同的五个个体测量了mRNA表达。

结论

各时间点之间的基因表达几乎没有有意义的差异。因此,使用标准实验室程序进行的微阵列测量可以是精确和定量的,并且不受显著随机生物学噪声的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afcc/2637424/5c4f7950fbbe/pone.0004486.g001.jpg

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