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Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs

Artificial small RNAs (art‐sRNAs) are 21‐nucleotide small RNAs (sRNAs) computationally designed to silence plant genes or pathogenic RNAs with high efficacy and specificity. They are typically produced in transgenic plants to induce silencing at the whole‐organism level, although their expression in...

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Autores principales: Cisneros, Adriana E., de la Torre‐Montaña, Ainhoa, Carbonell, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310713/
https://www.ncbi.nlm.nih.gov/pubmed/35277899
http://dx.doi.org/10.1111/tpj.15730
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author Cisneros, Adriana E.
de la Torre‐Montaña, Ainhoa
Carbonell, Alberto
author_facet Cisneros, Adriana E.
de la Torre‐Montaña, Ainhoa
Carbonell, Alberto
author_sort Cisneros, Adriana E.
collection PubMed
description Artificial small RNAs (art‐sRNAs) are 21‐nucleotide small RNAs (sRNAs) computationally designed to silence plant genes or pathogenic RNAs with high efficacy and specificity. They are typically produced in transgenic plants to induce silencing at the whole‐organism level, although their expression in selected tissues for inactivating genes in distal tissues has not been reported. Here, art‐sRNAs designed against the magnesium chelatase subunit CHLI‐encoding SULFUR gene (NbSu) were agroinfiltrated in Nicotiana benthamiana leaves, and the induction of local and systemic silencing was analyzed phenotypically by monitoring the appearance of the characteristic bleached phenotype, as well as molecularly by analyzing art‐sRNA processing, accumulation and targeting activity and efficacy. We found that the two classes of art‐sRNAs, artificial microRNAs (amiRNAs) and synthetic trans‐acting small interfering RNAs (syn‐tasiRNAs), are able to induce systemic silencing of NbSu, which requires high art‐sRNA expression in the vicinity of the leaf petiole but is independent on the production of secondary sRNAs from NbSu mRNAs. Moreover, we revealed that 21‐nucleotide amiRNA and syn‐tasiRNA duplexes, and not their precursors, are the molecules moving between cells and through the phloem to systemically silence NbSu in upper leaves. In sum, our results indicate that 21‐nucleotide art‐sRNAs can move throughout the plant to silence plant genes in tissues different from where they are produced. This highlights the biotechnological potential of art‐sRNAs, which might be applied locally for triggering whole‐plant and highly specific silencing to regulate gene expression or induce resistance against pathogenic RNAs in next‐generation crops. The present study demonstrates that artificial small RNAs, such as artificial microRNAs and synthetic trans‐acting small interfering RNAs, can move long distances in plants as 21‐nucleotide duplexes, specifically silencing endogenous genes in tissues different from where they are applied. This highlights the biotechnological potential of artificial small RNAs, which might be applied locally for triggering whole‐plant, highly specific silencing to regulate gene expression or induce resistance against pathogenic RNAs in next‐generation crops.
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spelling pubmed-93107132022-07-29 Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs Cisneros, Adriana E. de la Torre‐Montaña, Ainhoa Carbonell, Alberto Plant J Original Articles Artificial small RNAs (art‐sRNAs) are 21‐nucleotide small RNAs (sRNAs) computationally designed to silence plant genes or pathogenic RNAs with high efficacy and specificity. They are typically produced in transgenic plants to induce silencing at the whole‐organism level, although their expression in selected tissues for inactivating genes in distal tissues has not been reported. Here, art‐sRNAs designed against the magnesium chelatase subunit CHLI‐encoding SULFUR gene (NbSu) were agroinfiltrated in Nicotiana benthamiana leaves, and the induction of local and systemic silencing was analyzed phenotypically by monitoring the appearance of the characteristic bleached phenotype, as well as molecularly by analyzing art‐sRNA processing, accumulation and targeting activity and efficacy. We found that the two classes of art‐sRNAs, artificial microRNAs (amiRNAs) and synthetic trans‐acting small interfering RNAs (syn‐tasiRNAs), are able to induce systemic silencing of NbSu, which requires high art‐sRNA expression in the vicinity of the leaf petiole but is independent on the production of secondary sRNAs from NbSu mRNAs. Moreover, we revealed that 21‐nucleotide amiRNA and syn‐tasiRNA duplexes, and not their precursors, are the molecules moving between cells and through the phloem to systemically silence NbSu in upper leaves. In sum, our results indicate that 21‐nucleotide art‐sRNAs can move throughout the plant to silence plant genes in tissues different from where they are produced. This highlights the biotechnological potential of art‐sRNAs, which might be applied locally for triggering whole‐plant and highly specific silencing to regulate gene expression or induce resistance against pathogenic RNAs in next‐generation crops. The present study demonstrates that artificial small RNAs, such as artificial microRNAs and synthetic trans‐acting small interfering RNAs, can move long distances in plants as 21‐nucleotide duplexes, specifically silencing endogenous genes in tissues different from where they are applied. This highlights the biotechnological potential of artificial small RNAs, which might be applied locally for triggering whole‐plant, highly specific silencing to regulate gene expression or induce resistance against pathogenic RNAs in next‐generation crops. John Wiley and Sons Inc. 2022-03-27 2022-05 /pmc/articles/PMC9310713/ /pubmed/35277899 http://dx.doi.org/10.1111/tpj.15730 Text en © 2022 The Authors. The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Cisneros, Adriana E.
de la Torre‐Montaña, Ainhoa
Carbonell, Alberto
Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs
title Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs
title_full Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs
title_fullStr Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs
title_full_unstemmed Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs
title_short Systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small RNAs
title_sort systemic silencing of an endogenous plant gene by two classes of mobile 21‐nucleotide artificial small rnas
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310713/
https://www.ncbi.nlm.nih.gov/pubmed/35277899
http://dx.doi.org/10.1111/tpj.15730
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