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Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA

MicroRNAs (miRNAs) are a class of endogenous short noncoding RNA. They regulate gene expression and function, essential to biological processes. It is necessary to develop an efficient detection method to determine these valuable biomarkers for the diagnosis of cancers. In this paper, we proposed a...

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Detalles Bibliográficos
Autores principales: Niu, Chenqi, Liu, Juewen, Xing, Xinhui, Zhang, Chong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAAS 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085249/
https://www.ncbi.nlm.nih.gov/pubmed/37849464
http://dx.doi.org/10.34133/bdr.0010
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author Niu, Chenqi
Liu, Juewen
Xing, Xinhui
Zhang, Chong
author_facet Niu, Chenqi
Liu, Juewen
Xing, Xinhui
Zhang, Chong
author_sort Niu, Chenqi
collection PubMed
description MicroRNAs (miRNAs) are a class of endogenous short noncoding RNA. They regulate gene expression and function, essential to biological processes. It is necessary to develop an efficient detection method to determine these valuable biomarkers for the diagnosis of cancers. In this paper, we proposed a general and rapid method for sensitive and quantitative detection of miRNA by combining CRISPR–Cas12a and rolling circle amplification (RCA) with the precircularized probe. Eventually, the detection of miRNA-21 could be completed in 70 min with a limit of detection of 8.1 pM with high specificity. The reaction time was reduced by almost 4 h from more than 5 h to 70 min, which makes detection more efficient. This design improves the efficiency of CRISPR–Cas and RCA-based sensing strategy and shows great potential in lab-based detection and point-of-care test.
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spelling pubmed-100852492023-10-17 Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA Niu, Chenqi Liu, Juewen Xing, Xinhui Zhang, Chong Biodes Res Research Article MicroRNAs (miRNAs) are a class of endogenous short noncoding RNA. They regulate gene expression and function, essential to biological processes. It is necessary to develop an efficient detection method to determine these valuable biomarkers for the diagnosis of cancers. In this paper, we proposed a general and rapid method for sensitive and quantitative detection of miRNA by combining CRISPR–Cas12a and rolling circle amplification (RCA) with the precircularized probe. Eventually, the detection of miRNA-21 could be completed in 70 min with a limit of detection of 8.1 pM with high specificity. The reaction time was reduced by almost 4 h from more than 5 h to 70 min, which makes detection more efficient. This design improves the efficiency of CRISPR–Cas and RCA-based sensing strategy and shows great potential in lab-based detection and point-of-care test. AAAS 2023-03-27 /pmc/articles/PMC10085249/ /pubmed/37849464 http://dx.doi.org/10.34133/bdr.0010 Text en Copyright © 2023 Chenqi Niu et al. https://creativecommons.org/licenses/by/4.0/Exclusive licensee Nanjing Agricultural University. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY 4.0) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Niu, Chenqi
Liu, Juewen
Xing, Xinhui
Zhang, Chong
Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA
title Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA
title_full Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA
title_fullStr Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA
title_full_unstemmed Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA
title_short Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA
title_sort exploring the trans-cleavage activity with rolling circle amplification for fast detection of mirna
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085249/
https://www.ncbi.nlm.nih.gov/pubmed/37849464
http://dx.doi.org/10.34133/bdr.0010
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