Microfluidics-based digital quantitative PCR for single-cell small RNA quantification†
Author(s) -
Tian Yu,
Chong Tang,
Ying Zhang,
Ruirui Zhang,
Wei Yan
Publication year - 2017
Publication title -
biology of reproduction
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.366
H-Index - 180
eISSN - 1529-7268
pISSN - 0006-3363
DOI - 10.1093/biolre/iox102
Subject(s) - biology , microrna , digital polymerase chain reaction , computational biology , real time polymerase chain reaction , microfluidics , rna , quantitative assessment , polymerase chain reaction , genetics , gene , nanotechnology , materials science , management , economics
Quantitative analyses of small RNAs at the single-cell level have been challenging because of 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.
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