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In vivo DNA methylation editing in zebrafish
The CRISPR/dCas9-based epigenome editing technique has driven much attention. Fused with a catalytic domain from Dnmt or Tet protein, the CRISPR/dCas9-DnmtCD or -TetCD systems possess the targeted DNA methylation editing ability and have established a series of in vitro and in vivo disease models. H...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10038036/ https://www.ncbi.nlm.nih.gov/pubmed/36945831 http://dx.doi.org/10.1080/15592294.2023.2192326 |
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author | Liang, Fang Dong, Zijiong Ye, Jianmin Hu, Wei Bhandari, Ramji Kumar Mai, Kangsen Wang, Xuegeng |
author_facet | Liang, Fang Dong, Zijiong Ye, Jianmin Hu, Wei Bhandari, Ramji Kumar Mai, Kangsen Wang, Xuegeng |
author_sort | Liang, Fang |
collection | PubMed |
description | The CRISPR/dCas9-based epigenome editing technique has driven much attention. Fused with a catalytic domain from Dnmt or Tet protein, the CRISPR/dCas9-DnmtCD or -TetCD systems possess the targeted DNA methylation editing ability and have established a series of in vitro and in vivo disease models. However, no publication has been reported on zebrafish (Danio rerio), an important animal model in biomedicine. The present study demonstrated that CRISPR/dCas9-Dnmt7 and -Tet2 catalytic domain fusions could site-specifically edit genomic DNA methylation in vivo in zebrafish and may serve as an efficient toolkit for DNA methylation editing in the zebrafish model. |
format | Online Article Text |
id | pubmed-10038036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-100380362023-03-25 In vivo DNA methylation editing in zebrafish Liang, Fang Dong, Zijiong Ye, Jianmin Hu, Wei Bhandari, Ramji Kumar Mai, Kangsen Wang, Xuegeng Epigenetics Brief Report The CRISPR/dCas9-based epigenome editing technique has driven much attention. Fused with a catalytic domain from Dnmt or Tet protein, the CRISPR/dCas9-DnmtCD or -TetCD systems possess the targeted DNA methylation editing ability and have established a series of in vitro and in vivo disease models. However, no publication has been reported on zebrafish (Danio rerio), an important animal model in biomedicine. The present study demonstrated that CRISPR/dCas9-Dnmt7 and -Tet2 catalytic domain fusions could site-specifically edit genomic DNA methylation in vivo in zebrafish and may serve as an efficient toolkit for DNA methylation editing in the zebrafish model. Taylor & Francis 2023-03-22 /pmc/articles/PMC10038036/ /pubmed/36945831 http://dx.doi.org/10.1080/15592294.2023.2192326 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Brief Report Liang, Fang Dong, Zijiong Ye, Jianmin Hu, Wei Bhandari, Ramji Kumar Mai, Kangsen Wang, Xuegeng In vivo DNA methylation editing in zebrafish |
title | In vivo DNA methylation editing in zebrafish |
title_full | In vivo DNA methylation editing in zebrafish |
title_fullStr | In vivo DNA methylation editing in zebrafish |
title_full_unstemmed | In vivo DNA methylation editing in zebrafish |
title_short | In vivo DNA methylation editing in zebrafish |
title_sort | in vivo dna methylation editing in zebrafish |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10038036/ https://www.ncbi.nlm.nih.gov/pubmed/36945831 http://dx.doi.org/10.1080/15592294.2023.2192326 |
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