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Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica

Apple necrotic mosaic virus (ApNMV) is highly associated with the occurrence of apple mosaic disease in China. However, ApNMV–host interactions and defence mechanisms of host plants against this virus are poorly studied. Here, we report that nitrate treatment restrains ApNMV genomic RNA accumulation...

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Autores principales: Zhang, Zhenlu, Xie, Yin‐Huan, Sun, Ping, Zhang, Fu‐Jun, Zheng, Peng‐Fei, Wang, Xiao‐Fei, You, Chun‐Xiang, Hao, Yu‐Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828459/
https://www.ncbi.nlm.nih.gov/pubmed/34837323
http://dx.doi.org/10.1111/mpp.13166
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author Zhang, Zhenlu
Xie, Yin‐Huan
Sun, Ping
Zhang, Fu‐Jun
Zheng, Peng‐Fei
Wang, Xiao‐Fei
You, Chun‐Xiang
Hao, Yu‐Jin
author_facet Zhang, Zhenlu
Xie, Yin‐Huan
Sun, Ping
Zhang, Fu‐Jun
Zheng, Peng‐Fei
Wang, Xiao‐Fei
You, Chun‐Xiang
Hao, Yu‐Jin
author_sort Zhang, Zhenlu
collection PubMed
description Apple necrotic mosaic virus (ApNMV) is highly associated with the occurrence of apple mosaic disease in China. However, ApNMV–host interactions and defence mechanisms of host plants against this virus are poorly studied. Here, we report that nitrate treatment restrains ApNMV genomic RNA accumulation by destabilizing viral replication protein 1a through the MdBT2‐mediated ubiquitin‐proteasome pathway. MdBT2, a nitrate‐responsive BTB/TAZ domain‐containing protein, was identified in a yeast two‐hybrid screen of an apple cDNA library using viral protein 1a as bait, and 1a was further confirmed to interact with MdBT2 both in vivo and in vitro. It was further verified that MdBT2 promoted the ubiquitination and degradation of viral protein 1a through the ubiquitin‐proteasome pathway in an MdCUL3A‐independent manner. Viral genomic RNA accumulation was reduced in MdBT2‐overexpressing transgenic apple leaves but enhanced in MdBT2‐antisense leaves compared to the wild type. Moreover, MdBT2 was found to interfere with the interaction between viral replication proteins 1a and 2a(pol) by competitively interacting with 1a. Taken together, our results demonstrate that nitrate‐inducible MdBT2 functions as a limiting factor in ApNMV viral RNA accumulation by promoting the ubiquitination and degradation of viral protein 1a and interfering with interactions between viral replication proteins.
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spelling pubmed-88284592022-02-11 Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica Zhang, Zhenlu Xie, Yin‐Huan Sun, Ping Zhang, Fu‐Jun Zheng, Peng‐Fei Wang, Xiao‐Fei You, Chun‐Xiang Hao, Yu‐Jin Mol Plant Pathol Original Articles Apple necrotic mosaic virus (ApNMV) is highly associated with the occurrence of apple mosaic disease in China. However, ApNMV–host interactions and defence mechanisms of host plants against this virus are poorly studied. Here, we report that nitrate treatment restrains ApNMV genomic RNA accumulation by destabilizing viral replication protein 1a through the MdBT2‐mediated ubiquitin‐proteasome pathway. MdBT2, a nitrate‐responsive BTB/TAZ domain‐containing protein, was identified in a yeast two‐hybrid screen of an apple cDNA library using viral protein 1a as bait, and 1a was further confirmed to interact with MdBT2 both in vivo and in vitro. It was further verified that MdBT2 promoted the ubiquitination and degradation of viral protein 1a through the ubiquitin‐proteasome pathway in an MdCUL3A‐independent manner. Viral genomic RNA accumulation was reduced in MdBT2‐overexpressing transgenic apple leaves but enhanced in MdBT2‐antisense leaves compared to the wild type. Moreover, MdBT2 was found to interfere with the interaction between viral replication proteins 1a and 2a(pol) by competitively interacting with 1a. Taken together, our results demonstrate that nitrate‐inducible MdBT2 functions as a limiting factor in ApNMV viral RNA accumulation by promoting the ubiquitination and degradation of viral protein 1a and interfering with interactions between viral replication proteins. John Wiley and Sons Inc. 2021-11-26 /pmc/articles/PMC8828459/ /pubmed/34837323 http://dx.doi.org/10.1111/mpp.13166 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-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Zhang, Zhenlu
Xie, Yin‐Huan
Sun, Ping
Zhang, Fu‐Jun
Zheng, Peng‐Fei
Wang, Xiao‐Fei
You, Chun‐Xiang
Hao, Yu‐Jin
Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica
title Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica
title_full Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica
title_fullStr Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica
title_full_unstemmed Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica
title_short Nitrate‐inducible MdBT2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in Malus domestica
title_sort nitrate‐inducible mdbt2 acts as a restriction factor to limit apple necrotic mosaic virus genome replication in malus domestica
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828459/
https://www.ncbi.nlm.nih.gov/pubmed/34837323
http://dx.doi.org/10.1111/mpp.13166
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