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The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7
Bunyaviruses cleave host cellular mRNAs to acquire cap structures for their own mRNAs in a process called cap‐snatching. How bunyaviruses interact with cellular mRNA surveillance pathways such as nonsense‐mediated decay (NMD) during cap‐snatching remains poorly understood, especially in plants. Rice...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916216/ https://www.ncbi.nlm.nih.gov/pubmed/34954877 http://dx.doi.org/10.1111/mpp.13179 |
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author | Jin, Jing She, Yuanyuan Qiu, Ping Lin, Wenzhong Zhang, Wenwen Zhang, Jie Wu, Zujian Du, Zhenguo |
author_facet | Jin, Jing She, Yuanyuan Qiu, Ping Lin, Wenzhong Zhang, Wenwen Zhang, Jie Wu, Zujian Du, Zhenguo |
author_sort | Jin, Jing |
collection | PubMed |
description | Bunyaviruses cleave host cellular mRNAs to acquire cap structures for their own mRNAs in a process called cap‐snatching. How bunyaviruses interact with cellular mRNA surveillance pathways such as nonsense‐mediated decay (NMD) during cap‐snatching remains poorly understood, especially in plants. Rice stripe virus (RSV) is a plant bunyavirus threatening rice production in East Asia. Here, with a newly developed system allowing us to present defined mRNAs to RSV in Nicotiana benthamiana, we found that the frequency of RSV to target nonsense mRNAs (nsRNAs) during cap‐snatching was much lower than its frequency to target normal mRNAs. The frequency of RSV to target nsRNAs was increased by virus‐induced gene silencing of UPF1 or SMG7, each encoding a protein component involved in early steps of NMD (in an rdr6 RNAi background). Coincidently, RSV accumulation was increased in the UPF1‐ or SMG7‐silenced plants. These data indicated that the frequency of RSV to target nsRNAs during cap‐snatching is restricted by NMD. By restricting the frequency of RSV to target nsRNAs, NMD may impose a constraint to the overall cap‐snatching efficiency of RSV. Besides a deeper understanding for the cap‐snatching of RSV, these findings point to a novel role of NMD in plant–bunyavirus interactions. |
format | Online Article Text |
id | pubmed-8916216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89162162022-03-18 The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7 Jin, Jing She, Yuanyuan Qiu, Ping Lin, Wenzhong Zhang, Wenwen Zhang, Jie Wu, Zujian Du, Zhenguo Mol Plant Pathol Short Communication Bunyaviruses cleave host cellular mRNAs to acquire cap structures for their own mRNAs in a process called cap‐snatching. How bunyaviruses interact with cellular mRNA surveillance pathways such as nonsense‐mediated decay (NMD) during cap‐snatching remains poorly understood, especially in plants. Rice stripe virus (RSV) is a plant bunyavirus threatening rice production in East Asia. Here, with a newly developed system allowing us to present defined mRNAs to RSV in Nicotiana benthamiana, we found that the frequency of RSV to target nonsense mRNAs (nsRNAs) during cap‐snatching was much lower than its frequency to target normal mRNAs. The frequency of RSV to target nsRNAs was increased by virus‐induced gene silencing of UPF1 or SMG7, each encoding a protein component involved in early steps of NMD (in an rdr6 RNAi background). Coincidently, RSV accumulation was increased in the UPF1‐ or SMG7‐silenced plants. These data indicated that the frequency of RSV to target nsRNAs during cap‐snatching is restricted by NMD. By restricting the frequency of RSV to target nsRNAs, NMD may impose a constraint to the overall cap‐snatching efficiency of RSV. Besides a deeper understanding for the cap‐snatching of RSV, these findings point to a novel role of NMD in plant–bunyavirus interactions. John Wiley and Sons Inc. 2021-12-26 /pmc/articles/PMC8916216/ /pubmed/34954877 http://dx.doi.org/10.1111/mpp.13179 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology 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 | Short Communication Jin, Jing She, Yuanyuan Qiu, Ping Lin, Wenzhong Zhang, Wenwen Zhang, Jie Wu, Zujian Du, Zhenguo The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7 |
title | The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7
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title_full | The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7
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title_fullStr | The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7
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title_full_unstemmed | The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7
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title_short | The cap‐snatching frequency of a plant bunyavirus from nonsense mRNAs is low but is increased by silencing of UPF1 or SMG7
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title_sort | cap‐snatching frequency of a plant bunyavirus from nonsense mrnas is low but is increased by silencing of upf1 or smg7 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916216/ https://www.ncbi.nlm.nih.gov/pubmed/34954877 http://dx.doi.org/10.1111/mpp.13179 |
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