A multiplex RNA quantification method to determine the absolute amounts of mRNA without reverse transcription

被引:2
|
作者
Yokomori, Maasa [1 ]
Gotoh, Osamu [1 ]
Murakami, Yasufumi [2 ]
Fujimoto, Kenzo [3 ]
Suyama, Akira [1 ]
机构
[1] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Meguro Ku, 3-8-1 Komaba, Tokyo 1538902, Japan
[2] Tokyo Univ Sci, Grad Sch Ind Sci & Technol, Dept Biol Sci & Technol, 2641 Yamazaki, Noda, Chiba 2788510, Japan
[3] Japan Adv Inst Sci & Technol, Sch Mat Sci, 1-1 Asahidai, Nomi, Ishikawa 9231292, Japan
关键词
Quantification method; mRNA; Multiplex assay; Microarray; Transcriptome; Gene expression; POLYNUCLEOTIDE LIGASE; BACTERIOPHAGE-LAMBDA; EXPRESSION; ASSAY;
D O I
10.1016/j.ab.2017.10.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a highly sensitive microarray-based method that determines the absolute amounts of mRNA in a total RNA sample in a multiplex manner without reverse transcription. This direct mRNA measurement promotes high-throughput testing and reduces bias in transcriptome analyses. Furthermore, quantification of the absolute amount of mRNA allows transcriptome analysis without common controls or additional, complicated normalization. The method, called Photo-DEAN, was validated using chemically synthesized RNAs of known quantities and mouse liver total RNA samples. We found that the absolute amounts of mRNA were successfully measured without the cDNA synthesis step, with a sensitivity of 15 zmol achieved in 7 h.
引用
收藏
页码:96 / 103
页数:8
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