Microfluidics-based digital quantitative PCR for single-cell small RNA quantification

被引:7
|
作者
Yu, Tian [1 ]
Tang, Chong [1 ]
Zhang, Ying [1 ]
Zhang, Ruirui [1 ]
Yan, Wei [1 ,2 ]
机构
[1] Univ Nevada, Dept Physiol & Cell Biol, Reno Sch Med, 1664 North Virginia St,MS-575, Reno, NV 89557 USA
[2] Univ Nevada, Dept Biol, Reno Sch Med, Reno, NV 89557 USA
关键词
small RNA; RNA quantification; digital PCR; sperm; germ cells; fertility; REAL-TIME PCR; ABSOLUTE QUANTIFICATION; HOUSEKEEPING GENES; PATERNAL STRESS; SPERM; MICRORNA; EXPRESSION; FERTILIZATION; FRAGMENTS; TESTES;
D O I
10.1093/biolre/iox102
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
limited sensitivity and specificity of conventional real-time quantitative PCR methods. A digital quantitative PCR (dqPCR) method for miRNA quantification has been developed, but it requires the use of proprietary stem-loop primers and only applies to miRNA quantification. Here, we report a microfluidics-based dqPCR (mdqPCR) method, which takes advantage of the Fluidigm BioMark HD system for both template partition and the subsequent high-throughput dqPCR. Our mdqPCR method demonstrated excellent sensitivity and reproducibility suitable for quantitative analyses of not only miRNAs but also all other small RNA species at the single-cell level. Using this method, we discovered that each sperm has a unique miRNA profile. Summary Sentence We report a novel digital quantitative PCR method for single-cell small RNA analyses.
引用
收藏
页码:490 / 496
页数:7
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