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Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV

To establish a successful infection, a virus needs to replicate and move cell-to-cell efficiently. We investigated whether one of the genes upregulated in Nicotiana benthamiana after Bamboo mosaic virus (BaMV) inoculation was involved in regulating virus movement. We revealed the gene to be a plasma...

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Autores principales: Huang, Ying-Ping, Huang, Ying-Wen, Chen, I-Hsuan, Shenkwen, Lin-Ling, Hsu, Yau-Huei, Tsai, Ching-Hsiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853580/
https://www.ncbi.nlm.nih.gov/pubmed/28992255
http://dx.doi.org/10.1093/jxb/erx307
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author Huang, Ying-Ping
Huang, Ying-Wen
Chen, I-Hsuan
Shenkwen, Lin-Ling
Hsu, Yau-Huei
Tsai, Ching-Hsiu
author_facet Huang, Ying-Ping
Huang, Ying-Wen
Chen, I-Hsuan
Shenkwen, Lin-Ling
Hsu, Yau-Huei
Tsai, Ching-Hsiu
author_sort Huang, Ying-Ping
collection PubMed
description To establish a successful infection, a virus needs to replicate and move cell-to-cell efficiently. We investigated whether one of the genes upregulated in Nicotiana benthamiana after Bamboo mosaic virus (BaMV) inoculation was involved in regulating virus movement. We revealed the gene to be a plasma membrane-associated cation-binding protein 1-like protein, designated NbPCaP1L. The expression of NbPCaP1L in N. benthamiana was knocked down using Tobacco rattle virus-based gene silencing and consequently the accumulation of BaMV increased significantly to that of control plants. Further analysis indicated no significant difference in the accumulation of BaMV in NbPCaP1L knockdown and control protoplasts, suggesting NbPCaP1L may affect cell-to-cell movement of BaMV. Using a viral vector expressing green fluorescent protein in the knockdown plants, the mean area of viral focus, as determined by fluorescence, was found to be larger in NbPCaP1L knockdown plants. Orange fluorescence protein (OFP)-fused NbPCaP1L, NbPCaP1L-OFP, was expressed in N. benthamiana and reduced the accumulation of BaMV to 46%. To reveal the possible interaction of viral protein with NbPCaP1L, we performed yeast two-hybrid and co-immunoprecipitation experiments. The results indicated that NbPCaP1L interacted with BaMV replicase. The results also suggested that NbPCaP1L could trap the BaMV movement RNP complex via interaction with the viral replicase in the complex and so restricted viral cell-to-cell movement.
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spelling pubmed-58535802018-07-25 Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV Huang, Ying-Ping Huang, Ying-Wen Chen, I-Hsuan Shenkwen, Lin-Ling Hsu, Yau-Huei Tsai, Ching-Hsiu J Exp Bot Research Papers To establish a successful infection, a virus needs to replicate and move cell-to-cell efficiently. We investigated whether one of the genes upregulated in Nicotiana benthamiana after Bamboo mosaic virus (BaMV) inoculation was involved in regulating virus movement. We revealed the gene to be a plasma membrane-associated cation-binding protein 1-like protein, designated NbPCaP1L. The expression of NbPCaP1L in N. benthamiana was knocked down using Tobacco rattle virus-based gene silencing and consequently the accumulation of BaMV increased significantly to that of control plants. Further analysis indicated no significant difference in the accumulation of BaMV in NbPCaP1L knockdown and control protoplasts, suggesting NbPCaP1L may affect cell-to-cell movement of BaMV. Using a viral vector expressing green fluorescent protein in the knockdown plants, the mean area of viral focus, as determined by fluorescence, was found to be larger in NbPCaP1L knockdown plants. Orange fluorescence protein (OFP)-fused NbPCaP1L, NbPCaP1L-OFP, was expressed in N. benthamiana and reduced the accumulation of BaMV to 46%. To reveal the possible interaction of viral protein with NbPCaP1L, we performed yeast two-hybrid and co-immunoprecipitation experiments. The results indicated that NbPCaP1L interacted with BaMV replicase. The results also suggested that NbPCaP1L could trap the BaMV movement RNP complex via interaction with the viral replicase in the complex and so restricted viral cell-to-cell movement. Oxford University Press 2017-10-13 2017-08-29 /pmc/articles/PMC5853580/ /pubmed/28992255 http://dx.doi.org/10.1093/jxb/erx307 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Huang, Ying-Ping
Huang, Ying-Wen
Chen, I-Hsuan
Shenkwen, Lin-Ling
Hsu, Yau-Huei
Tsai, Ching-Hsiu
Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV
title Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV
title_full Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV
title_fullStr Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV
title_full_unstemmed Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV
title_short Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV
title_sort plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of bamv
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853580/
https://www.ncbi.nlm.nih.gov/pubmed/28992255
http://dx.doi.org/10.1093/jxb/erx307
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