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CRISPR as a Diagnostic Tool

Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas system has recently gained growing attention as a diagnostic tool due to its capability of specific gene targeting. It consists of Cas enzymes and a guide RNA (gRNA) that can cleave the target DNA or RNA based on the sequence of...

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Autores principales: Kim, Seohyun, Ji, Sangmin, Koh, Hye Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391464/
https://www.ncbi.nlm.nih.gov/pubmed/34439828
http://dx.doi.org/10.3390/biom11081162
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author Kim, Seohyun
Ji, Sangmin
Koh, Hye Ran
author_facet Kim, Seohyun
Ji, Sangmin
Koh, Hye Ran
author_sort Kim, Seohyun
collection PubMed
description Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas system has recently gained growing attention as a diagnostic tool due to its capability of specific gene targeting. It consists of Cas enzymes and a guide RNA (gRNA) that can cleave the target DNA or RNA based on the sequence of the gRNA, making it an attractive genetic engineering technique. In addition to the target-specific binding and cleavage, the trans-cleavage activity was reported for some Cas proteins, including Cas12a and Cas13a, which is to cleave the surrounding single-stranded DNA or RNA upon the target binding of Cas-gRNA complex. All these activities of the CRISPR-Cas system are based on its target-specific binding, making it applied to develop diagnostic methods by detecting the disease-related gene as well as microRNAs and the genetic variations such as single nucleotide polymorphism and DNA methylation. Moreover, it can be applied to detect the non-nucleic acids target such as proteins. In this review, we cover the various CRISPR-based diagnostic methods by focusing on the activity of the CRISPR-Cas system and the form of the target. The CRISPR-based diagnostic methods without target amplification are also introduced briefly.
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spelling pubmed-83914642021-08-28 CRISPR as a Diagnostic Tool Kim, Seohyun Ji, Sangmin Koh, Hye Ran Biomolecules Review Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas system has recently gained growing attention as a diagnostic tool due to its capability of specific gene targeting. It consists of Cas enzymes and a guide RNA (gRNA) that can cleave the target DNA or RNA based on the sequence of the gRNA, making it an attractive genetic engineering technique. In addition to the target-specific binding and cleavage, the trans-cleavage activity was reported for some Cas proteins, including Cas12a and Cas13a, which is to cleave the surrounding single-stranded DNA or RNA upon the target binding of Cas-gRNA complex. All these activities of the CRISPR-Cas system are based on its target-specific binding, making it applied to develop diagnostic methods by detecting the disease-related gene as well as microRNAs and the genetic variations such as single nucleotide polymorphism and DNA methylation. Moreover, it can be applied to detect the non-nucleic acids target such as proteins. In this review, we cover the various CRISPR-based diagnostic methods by focusing on the activity of the CRISPR-Cas system and the form of the target. The CRISPR-based diagnostic methods without target amplification are also introduced briefly. MDPI 2021-08-06 /pmc/articles/PMC8391464/ /pubmed/34439828 http://dx.doi.org/10.3390/biom11081162 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kim, Seohyun
Ji, Sangmin
Koh, Hye Ran
CRISPR as a Diagnostic Tool
title CRISPR as a Diagnostic Tool
title_full CRISPR as a Diagnostic Tool
title_fullStr CRISPR as a Diagnostic Tool
title_full_unstemmed CRISPR as a Diagnostic Tool
title_short CRISPR as a Diagnostic Tool
title_sort crispr as a diagnostic tool
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391464/
https://www.ncbi.nlm.nih.gov/pubmed/34439828
http://dx.doi.org/10.3390/biom11081162
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