A flexible microfluidic system for single-cell transcriptome profiling elucidates phased transcriptional regulators of cell cycle

被引:10
作者
Davey, Karen [1 ]
Wong, Daniel [2 ]
Konopacki, Filip [2 ]
Kwa, Eugene [1 ]
Ly, Tony [3 ]
Fiegler, Heike [2 ]
Sibley, Christopher R. [1 ,4 ,5 ,6 ]
机构
[1] Imperial Coll London, Dept Med, Div Brain Sci, London, England
[2] Dolomite Bio, Unit 3,Anglian Business Pk, Royston, England
[3] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh, Midlothian, Scotland
[4] Univ Edinburgh, Sch Biol Sci, Inst Quantitat Biol Biochem & Biotechnol, 1 George Sq, Edinburgh EH8 9JZ, Midlothian, Scotland
[5] Univ Edinburgh, Simons Initiat Developing Brain, Hugh Robson Bldg,George Sq, Edinburgh EH8 9XD, Midlothian, Scotland
[6] Univ Edinburgh, Ctr Discovery Brain Sci, Hugh Robson Bldg,George Sq, Edinburgh EH8 9XD, Midlothian, Scotland
基金
英国惠康基金;
关键词
NUCLEUS RNA-SEQ; EXPRESSION; GENE; PHOSPHORYLATION; QUANTIFICATION; IDENTIFICATION; DYNAMICS; SCREENS; TISSUES; MITOSIS;
D O I
10.1038/s41598-021-86070-z
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
Single cell transcriptome profiling has emerged as a breakthrough technology for the high-resolution understanding of complex cellular systems. Here we report a flexible, cost-effective and user-friendly droplet-based microfluidics system, called the Nadia Instrument, that can allow 3 ' mRNA capture of similar to 50,000 single cells or individual nuclei in a single run. The precise pressure-based system demonstrates highly reproducible droplet size, low doublet rates and high mRNA capture efficiencies that compare favorably in the field. Moreover, when combined with the Nadia Innovate, the system can be transformed into an adaptable setup that enables use of different buffers and barcoded bead configurations to facilitate diverse applications. Finally, by 3 ' mRNA profiling asynchronous human and mouse cells at different phases of the cell cycle, we demonstrate the system's ability to readily distinguish distinct cell populations and infer underlying transcriptional regulatory networks. Notably this provided supportive evidence for multiple transcription factors that had little or no known link to the cell cycle (e.g. DRAP1, ZKSCAN1 and CEBPZ). In summary, the Nadia platform represents a promising and flexible technology for future transcriptomic studies, and other related applications, at cell resolution.
引用
收藏
页数:13
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