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8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense

Gene silencing is an important biological strategy for studying gene functions, exploring disease mechanisms and developing therapeutics. 8–17 DNAzyme is of great potential for gene silencing, due to its higher RNA-cleaving activity. However, it is not generally used in practice, due to its divalent...

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Detalles Bibliográficos
Autores principales: Zhou, Zhongchun, Sun, Wen, Huang, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821912/
https://www.ncbi.nlm.nih.gov/pubmed/36615479
http://dx.doi.org/10.3390/molecules28010286
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author Zhou, Zhongchun
Sun, Wen
Huang, Zhen
author_facet Zhou, Zhongchun
Sun, Wen
Huang, Zhen
author_sort Zhou, Zhongchun
collection PubMed
description Gene silencing is an important biological strategy for studying gene functions, exploring disease mechanisms and developing therapeutics. 8–17 DNAzyme is of great potential for gene silencing, due to its higher RNA-cleaving activity. However, it is not generally used in practice, due to its divalent cation dependence and poor understanding of its cellular mechanisms. To address these issues, we have explored its activity in vitro and in cells and found that it can cleave RNA substrates under the simulated physiological conditions, and its gene-silencing activity is additionally enhanced by its RNase H compatibility, offering both cleavage and antisense activities in cells. Further, chemical modifications can facilitate its stability, substrate binding affinity and gene-silencing activity. Our research results suggest that this DNAzyme can demonstrate high levels of activities for both actions in cells, making it a useful tool for exploring biomedical applications.
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spelling pubmed-98219122023-01-07 8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense Zhou, Zhongchun Sun, Wen Huang, Zhen Molecules Article Gene silencing is an important biological strategy for studying gene functions, exploring disease mechanisms and developing therapeutics. 8–17 DNAzyme is of great potential for gene silencing, due to its higher RNA-cleaving activity. However, it is not generally used in practice, due to its divalent cation dependence and poor understanding of its cellular mechanisms. To address these issues, we have explored its activity in vitro and in cells and found that it can cleave RNA substrates under the simulated physiological conditions, and its gene-silencing activity is additionally enhanced by its RNase H compatibility, offering both cleavage and antisense activities in cells. Further, chemical modifications can facilitate its stability, substrate binding affinity and gene-silencing activity. Our research results suggest that this DNAzyme can demonstrate high levels of activities for both actions in cells, making it a useful tool for exploring biomedical applications. MDPI 2022-12-29 /pmc/articles/PMC9821912/ /pubmed/36615479 http://dx.doi.org/10.3390/molecules28010286 Text en © 2022 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 Article
Zhou, Zhongchun
Sun, Wen
Huang, Zhen
8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense
title 8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense
title_full 8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense
title_fullStr 8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense
title_full_unstemmed 8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense
title_short 8–17 DNAzyme Silencing Gene Expression in Cells via Cleavage and Antisense
title_sort 8–17 dnazyme silencing gene expression in cells via cleavage and antisense
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821912/
https://www.ncbi.nlm.nih.gov/pubmed/36615479
http://dx.doi.org/10.3390/molecules28010286
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