Abstract
MicroRNAs (miRNAs) and short RNA fragments (18–25 nt) are crucial biomarkers in biological research and disease diagnostics. However, their accurate and rapid detection remains a challenge, largely due to their low abundance, short length, and sequence similarities. In this study, we report on a highly sensitive, one-step RNA O-circle amplification (ROA) assay for rapid and accurate miRNA detection. The ROA assay commences with the hybridization of a circular probe with the test RNA, followed by a linear rolling circle amplification (RCA) using dUTP. This amplification process is facilitated by U-nick reactions, which lead to an exponential amplification for readout. Under optimized conditions, assays can be completed within an hour, producing an amplification yield up to the microgram level, with a detection limit as low as 0.15 fmol (6 pM). Notably, the ROA assay requires only one step, and the results can be easily read visually, making it user-friendly. This ROA assay has proven effective in detecting various miRNAs and phage ssRNA. Overall, the ROA assay offers a user-friendly, rapid, and accurate solution for miRNA detection.
Original language | English (US) |
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Pages (from-to) | 298-308 |
Number of pages | 11 |
Journal | aBIOTECH |
Volume | 5 |
Issue number | 3 |
DOIs | |
State | Published - Sep 2024 |
Keywords
- Fluorescence detection
- miRNA
- Rolling circle amplification (RCA)
- Sensitive detection
ASJC Scopus subject areas
- Biotechnology
- Molecular Biology
- Biochemistry, Genetics and Molecular Biology (miscellaneous)
- Genetics
- Agronomy and Crop Science
- Plant Science