4.7 Article

Low bias multiple displacement amplification with confinement effect based on agarose gel

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 413, 期 17, 页码 4397-4405

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03415-3

关键词

Multiple displacement amplification; Low melting agarose gel; Bias; Confinement effect

资金

  1. National Natural Science Foundation of China [81827901, 61801108]
  2. Natural Science Foundation of Jiangsu Province [BK20201148]

向作者/读者索取更多资源

An improved MDA method named gelMDA was proposed in this study, which significantly increased the efficiency and product yield of single-cell genome amplification, while reducing amplification bias. It showed great potential in single-cell RNA amplification and sequencing.
Multiple displacement amplification (MDA) is a popular single-cell whole-genome amplification (WGA) technique that can greatly improve the amplification efficiency of single-cell genomes. However, there is an inherent problem that cannot be completely solved, that is, the amplification bias. We here propose an improved MDA method based on low melting agarose gel, named gelMDA. Firstly, the agarose gel and solution were characterized with SEM and fluorescent reagent. Then, we used gelMDA for cDNA amplification in library preparation of RNA-seq, and conventional MDA was used as a comparison. The sensitivity, efficiency of gelMDA, and amplification bias were evaluated with fluorescence curve, product yield, and the sequencing results. Finally, gelMDA was used for single-cell transcriptome sequencing. The results showed that the sensitivity and product yield of gelMDA were significantly higher than those of conventional MDA. A lower coefficient of variation (CV) and a higher reproducibility were obtained from gelMDA sequencing results. A region of 30 mu m in diameter was amplified from the tissue sections and successfully sequenced. In conclusion, gelMDA obtained higher amplification efficiency and lower amplification bias in the present study. It suggested the great potential in single-cell RNA amplification and sequencing.

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