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基于电子微阵列的多重靶向基因表达谱分析和遗传分析。

Multiplexed, targeted gene expression profiling and genetic analysis on electronic microarrays.

作者信息

Weidenhammer Elaine M, Kahl Brenda F, Wang Ling, Wang Larry, Duhon Melanie, Jackson Jo Ann, Slater Matthew, Xu Xiao

机构信息

Department of Research and Development, Nanogen, Inc., 10398 Pacific Center Ct., San Diego, CA 92121, USA.

出版信息

Clin Chem. 2002 Nov;48(11):1873-82.

Abstract

BACKGROUND

Electronic microarrays comprise independent microelectrode test sites that can be electronically biased positive or negative, or left neutral, to move and concentrate charged molecules such as DNA and RNA to one or more test sites. We developed a protocol for multiplexed gene expression profiling of mRNA targets that uses electronic field-facilitated hybridization on electronic microarrays.

METHODS

A multiplexed, T7 RNA polymerase-mediated amplification method was used for expression profiling of target mRNAs from total cellular RNA; targets were detected by hybridization to sequence-specific capture oligonucleotides on electronic microarrays. Activation of individual test sites on the electronic microarray was used to target hybridization to designated subsets of sites and allow comparisons of target concentrations in different samples. We used multiplexed amplification and electronic field-facilitated hybridization to analyze expression of a model set of 10 target genes in the U937 cell line during lipopolysaccharide-mediated differentiation. Performance of multiple genetic analyses (single-nucleotide polymorphism detection, gene expression profiling, and splicing isoform detection) on a single electronic microarray was demonstrated using the ApoE and ApoER2 genes as a model system.

RESULTS

Targets were detected after a 2-min hybridization reaction. With noncomplementary capture probes, no signal was detectable. Twofold changes in target concentration were detectable throughout the ( approximately 64-fold) range of concentrations tested. Levels of 10 targets were analyzed side by side across seven time points. By confining electronic activation to subsets of test sites, polymorphism detection, expression profiling, and splicing isoform analysis were performed on a single electronic microarray.

CONCLUSIONS

Microelectronic array technology provides specific target detection and quantification with advantages over currently available methodologies for targeted gene expression profiling and combinatorial genomics testing.

摘要

背景

电子微阵列由独立的微电极测试位点组成,这些位点可通过电子方式设置为正偏压、负偏压或保持中性,以将诸如DNA和RNA等带电分子移动并浓缩到一个或多个测试位点。我们开发了一种用于mRNA靶标多重基因表达谱分析的方案,该方案利用电子微阵列上的电场辅助杂交技术。

方法

采用多重T7 RNA聚合酶介导的扩增方法对总细胞RNA中的靶标mRNA进行表达谱分析;通过与电子微阵列上的序列特异性捕获寡核苷酸杂交来检测靶标。利用电子微阵列上单个测试位点的激活,使杂交靶向指定的位点子集,并允许比较不同样品中靶标的浓度。我们使用多重扩增和电场辅助杂交技术分析了脂多糖介导的U937细胞系分化过程中一组10个靶标基因的表达。以载脂蛋白E(ApoE)和载脂蛋白E受体2(ApoER2)基因为模型系统,展示了在单个电子微阵列上进行多种遗传分析(单核苷酸多态性检测、基因表达谱分析和剪接异构体检测)的性能。

结果

经过2分钟的杂交反应后检测到靶标。使用非互补捕获探针时,未检测到信号。在整个测试浓度范围(约64倍)内均可检测到靶标浓度两倍的变化。在七个时间点并行分析了10个靶标的水平。通过将电子激活限制在测试位点的子集上,在单个电子微阵列上进行了多态性检测、表达谱分析和剪接异构体分析。

结论

微电子阵列技术提供了特异性靶标检测和定量,相对于目前用于靶向基因表达谱分析和组合基因组学检测的方法具有优势。

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