High-throughput microfluidic single-cell RT-qPCR

被引:345
作者
White, Adam K. [1 ]
VanInsberghe, Michael [1 ]
Petriv, Oleh I. [1 ,2 ]
Hamidi, Mani [1 ]
Sikorski, Darek [1 ,3 ,5 ]
Marra, Marco A. [4 ]
Piret, James [3 ,5 ]
Aparicio, Samuel [6 ,7 ]
Hansen, Carl L. [1 ,2 ]
机构
[1] Univ British Columbia, Ctr High Throughput Biol, Vancouver, BC V6T 1Z4, Canada
[2] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 1Z4, Canada
[3] Univ British Columbia, Dept Chem & Biol Engn, Vancouver, BC V6T 1Z4, Canada
[4] BC Canc Agcy, Michael Smith Genome Sci Ctr, Vancouver, BC V5Z 4S6, Canada
[5] Univ British Columbia, Michael Smith Labs, Vancouver, BC V6T 1Z4, Canada
[6] Ctr Translat & Appl Genom, Vancouver, BC V5Z 4E6, Canada
[7] Univ British Columbia, Dept Pathol, Vancouver, BC V6T 2B5, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
real-time PCR; lab on a chip; transcriptional noise; microRNA; single-cell diagnostics; EMBRYONIC STEM-CELLS; GENE-EXPRESSION ANALYSIS; MESSENGER-RNA MOLECULES; DIFFERENTIATION; RESOLUTION; MICRORNAS; CHIP;
D O I
10.1073/pnas.1019446108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A long-sought milestone in microfluidics research has been the development of integrated technology for scalable analysis of transcription in single cells. Here we present a fully integrated microfluidic device capable of performing high-precision RT-qPCR measurements of gene expression from hundreds of single cells per run. Our device executes all steps of single-cell processing, including cell capture, cell lysis, reverse transcription, and quantitative PCR. In addition to higher throughput and reduced cost, we show that nanoliter volume processing reduced measurement noise, increased sensitivity, and provided single nucleotide specificity. We apply this technology to 3,300 single-cell measurements of (i) miRNA expression in K562 cells, (ii) coregulation of a miRNA and one of its target transcripts during differentiation in embryonic stem cells, and (iii) single nucleotide variant detection in primary lobular breast cancer cells. The core functionality established here provides the foundation from which a variety of on-chip single-cell transcription analyses will be developed.
引用
收藏
页码:13999 / 14004
页数:6
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