Kuriyama Kentaro, Shintaku Hirofumi, Santiago Juan G
Department of Mechanical Engineering, Stanford University, Escondido, Stanford, CA, USA.
Department of Micro Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto, Japan.
Electrophoresis. 2015 Jul;36(14):1658-62. doi: 10.1002/elps.201500040. Epub 2015 May 20.
There is a substantial need for simultaneous analyses of RNA and DNA from individual single cells. Such analysis provides unique evidence of cell-to-cell differences and the correlation between gene expression and genomic mutation in highly heterogeneous cell populations. We present a novel microfluidic system that leverages isotachophoresis to fractionate and isolate cytoplasmic RNA and genomic DNA (gDNA) from single cells. The system uniquely enables independent, sequence-specific analyses of these critical markers. Our system uses a microfluidic chip with a simple geometry and four end-channel electrodes, and completes the entire process in <5 min, including lysis, purification, fractionation, and delivery to DNA and RNA output reservoirs, each containing high quality and purity aliquots with no measurable cross-contamination of cytoplasmic RNA versus gDNA. We demonstrate our system with simultaneous, sequence-specific quantitation using off-chip RT-qPCR and qPCR for simultaneous cytoplasmic RNA and gDNA analyses, respectively.
迫切需要对单个单细胞的RNA和DNA进行同步分析。这种分析为高度异质细胞群体中细胞间差异以及基因表达与基因组突变之间的相关性提供了独特的证据。我们提出了一种新型微流控系统,该系统利用等速电泳从单细胞中分离和分离细胞质RNA和基因组DNA(gDNA)。该系统独特地能够对这些关键标志物进行独立的、序列特异性分析。我们的系统使用具有简单几何形状和四个末端通道电极的微流控芯片,并在不到5分钟的时间内完成整个过程,包括裂解、纯化、分离以及输送到DNA和RNA输出储液器,每个储液器都含有高质量和高纯度的等分试样,细胞质RNA与gDNA之间没有可测量的交叉污染。我们通过使用芯片外RT-qPCR和qPCR分别对细胞质RNA和gDNA进行同步分析,以序列特异性定量的方式展示了我们的系统。