4.8 Article

Programmable Ligation-Transcription Circuit-Driven Cascade Amplification Machinery for Multiple Long Noncoding RNAs Detection in Lung Tissues

Journal

ANALYTICAL CHEMISTRY
Volume 94, Issue 30, Pages 10573-10578

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c02685

Keywords

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Funding

  1. National Natural Science Foundation of China [21735003]
  2. Award for Team Leader Program of Taishan Scholars of Shandong Province, China

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A simple method for simultaneous detection of multiple lncRNAs using programmable ligation-transcription circuits and single-molecule counting is developed in this study. The method shows high sensitivity and enables the measurement of multiple endogenous lncRNAs at the single-cell level, providing a promising platform for clinical diagnosis and biomedical research.
The measurement of long noncoding RNAs (lncRNAs) is essential to diagnosis and treatment of various diseases such as cancers. Herein, we develop a simple method to simultaneously detect multiple lncRNAs using programmable ligation-transcription circuit-driven cascade amplification and single-molecule counting. The presence of targets lncRNA HOTAIR and lncRNA MALAT1 activates the ligation-transcription circuits to produce two corresponding functional RNAs. The functional RNAs then cyclically initiate the digestion of signal probes by duplex-specific nuclease to liberate Cy5 and Cy3 molecules. After magnetic separation, the liberated Cy5 and Cy3 molecules are measured by single-molecule counting. In this assay, a single lncRNA can activate ligation-transcription circuit to generate abundant functional RNAs, endowing this assay with high sensitivity. Integration of single-molecule counting ensures the high sensitivity. This method shows extremely high sensitivity with a limit of detection (LOD) of 0.043 aM for HOX gene antisense intergenic RNA (lncRNA HOTAIR) and 0.126 aM for mammalian metastasis-related lung adenocarcinoma transcript 1 (lncRNA MALAT1). Importantly, this method enables simultaneous measurement of multiple endogenous lncRNAs at the single-cell level, and it may discriminate the expressions of various lncRNA in lung tumor tissues of nonsmall cell lung cancer (NSCLC) patients and their corresponding healthy adjacent tissues, offering a promising platform for clinical diagnosis and biomedical research.

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