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Strategies for mitochondrial gene editing

Mitochondria, as the energy factory of cells, participate in metabolism processes and play a critical role in the maintenance of human life activities. Mitochondria belong to semi-automatic organelles, which have their own genome different from nuclear genome. Mitochondrial DNA (mtDNA) mutations can...

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Detalles Bibliográficos
Autores principales: Yang, Xingbo, Jiang, Jiacheng, Li, Zongyu, Liang, Jiayi, Xiang, Yaozu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202187/
https://www.ncbi.nlm.nih.gov/pubmed/34188780
http://dx.doi.org/10.1016/j.csbj.2021.06.003
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author Yang, Xingbo
Jiang, Jiacheng
Li, Zongyu
Liang, Jiayi
Xiang, Yaozu
author_facet Yang, Xingbo
Jiang, Jiacheng
Li, Zongyu
Liang, Jiayi
Xiang, Yaozu
author_sort Yang, Xingbo
collection PubMed
description Mitochondria, as the energy factory of cells, participate in metabolism processes and play a critical role in the maintenance of human life activities. Mitochondria belong to semi-automatic organelles, which have their own genome different from nuclear genome. Mitochondrial DNA (mtDNA) mutations can cause a series of diseases and threaten human health. However, an effective approach to edit mitochondrial DNA, though long-desired, is lacking. In recent years, gene editing technologies, represented by restriction endonucleases (RE) technology, zinc finger nuclease (ZFN) technology, transcription activator-like effector nuclease (TALEN) technology, CRISPR system and pAgo-based system have been comprehensively explored, but the application of these technologies in mitochondrial gene editing is still to be explored and optimized. The present study highlights the progress and limitations of current mitochondrial gene editing technologies and approaches, and provides insights for development of novel strategies for future attempts.
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spelling pubmed-82021872021-06-28 Strategies for mitochondrial gene editing Yang, Xingbo Jiang, Jiacheng Li, Zongyu Liang, Jiayi Xiang, Yaozu Comput Struct Biotechnol J Review Mitochondria, as the energy factory of cells, participate in metabolism processes and play a critical role in the maintenance of human life activities. Mitochondria belong to semi-automatic organelles, which have their own genome different from nuclear genome. Mitochondrial DNA (mtDNA) mutations can cause a series of diseases and threaten human health. However, an effective approach to edit mitochondrial DNA, though long-desired, is lacking. In recent years, gene editing technologies, represented by restriction endonucleases (RE) technology, zinc finger nuclease (ZFN) technology, transcription activator-like effector nuclease (TALEN) technology, CRISPR system and pAgo-based system have been comprehensively explored, but the application of these technologies in mitochondrial gene editing is still to be explored and optimized. The present study highlights the progress and limitations of current mitochondrial gene editing technologies and approaches, and provides insights for development of novel strategies for future attempts. Research Network of Computational and Structural Biotechnology 2021-06-04 /pmc/articles/PMC8202187/ /pubmed/34188780 http://dx.doi.org/10.1016/j.csbj.2021.06.003 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Yang, Xingbo
Jiang, Jiacheng
Li, Zongyu
Liang, Jiayi
Xiang, Yaozu
Strategies for mitochondrial gene editing
title Strategies for mitochondrial gene editing
title_full Strategies for mitochondrial gene editing
title_fullStr Strategies for mitochondrial gene editing
title_full_unstemmed Strategies for mitochondrial gene editing
title_short Strategies for mitochondrial gene editing
title_sort strategies for mitochondrial gene editing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202187/
https://www.ncbi.nlm.nih.gov/pubmed/34188780
http://dx.doi.org/10.1016/j.csbj.2021.06.003
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