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CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana

Viruses interfere with and usurp host machinery and circumvent defense responses to create a suitable cellular environment for successful infection. This is usually achieved through interactions between viral proteins and host factors. Geminiviruses are a group of plant-infecting DNA viruses, of whi...

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Autores principales: Jia, Qi, Liu, Na, Xie, Ke, Dai, Yanwan, Han, Shaojie, Zhao, Xijuan, Qian, Lichao, Wang, Yunjing, Zhao, Jinping, Gorovits, Rena, Xie, Daoxin, Hong, Yiguo, Liu, Yule
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912122/
https://www.ncbi.nlm.nih.gov/pubmed/27315204
http://dx.doi.org/10.1371/journal.ppat.1005668
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author Jia, Qi
Liu, Na
Xie, Ke
Dai, Yanwan
Han, Shaojie
Zhao, Xijuan
Qian, Lichao
Wang, Yunjing
Zhao, Jinping
Gorovits, Rena
Xie, Daoxin
Hong, Yiguo
Liu, Yule
author_facet Jia, Qi
Liu, Na
Xie, Ke
Dai, Yanwan
Han, Shaojie
Zhao, Xijuan
Qian, Lichao
Wang, Yunjing
Zhao, Jinping
Gorovits, Rena
Xie, Daoxin
Hong, Yiguo
Liu, Yule
author_sort Jia, Qi
collection PubMed
description Viruses interfere with and usurp host machinery and circumvent defense responses to create a suitable cellular environment for successful infection. This is usually achieved through interactions between viral proteins and host factors. Geminiviruses are a group of plant-infecting DNA viruses, of which some contain a betasatellite, known as DNAβ. Here, we report that Cotton leaf curl Multan virus (CLCuMuV) uses its sole satellite-encoded protein βC1 to regulate the plant ubiquitination pathway for effective infection. We found that CLCuMu betasatellite (CLCuMuB) βC1 interacts with NbSKP1, and interrupts the interaction of NbSKP1s with NbCUL1. Silencing of either NbSKP1s or NbCUL1 enhances the accumulation of CLCuMuV genomic DNA and results in severe disease symptoms in plants. βC1 impairs the integrity of SCF(COI1) and the stabilization of GAI, a substrate of the SCF(SYL1) to hinder responses to jasmonates (JA) and gibberellins (GA). Moreover, JA treatment reduces viral accumulation and symptoms. These results suggest that CLCuMuB βC1 inhibits the ubiquitination function of SCF E3 ligases through interacting with NbSKP1s to enhance CLCuMuV infection and symptom induction in plants.
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spelling pubmed-49121222016-07-06 CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana Jia, Qi Liu, Na Xie, Ke Dai, Yanwan Han, Shaojie Zhao, Xijuan Qian, Lichao Wang, Yunjing Zhao, Jinping Gorovits, Rena Xie, Daoxin Hong, Yiguo Liu, Yule PLoS Pathog Research Article Viruses interfere with and usurp host machinery and circumvent defense responses to create a suitable cellular environment for successful infection. This is usually achieved through interactions between viral proteins and host factors. Geminiviruses are a group of plant-infecting DNA viruses, of which some contain a betasatellite, known as DNAβ. Here, we report that Cotton leaf curl Multan virus (CLCuMuV) uses its sole satellite-encoded protein βC1 to regulate the plant ubiquitination pathway for effective infection. We found that CLCuMu betasatellite (CLCuMuB) βC1 interacts with NbSKP1, and interrupts the interaction of NbSKP1s with NbCUL1. Silencing of either NbSKP1s or NbCUL1 enhances the accumulation of CLCuMuV genomic DNA and results in severe disease symptoms in plants. βC1 impairs the integrity of SCF(COI1) and the stabilization of GAI, a substrate of the SCF(SYL1) to hinder responses to jasmonates (JA) and gibberellins (GA). Moreover, JA treatment reduces viral accumulation and symptoms. These results suggest that CLCuMuB βC1 inhibits the ubiquitination function of SCF E3 ligases through interacting with NbSKP1s to enhance CLCuMuV infection and symptom induction in plants. Public Library of Science 2016-06-17 /pmc/articles/PMC4912122/ /pubmed/27315204 http://dx.doi.org/10.1371/journal.ppat.1005668 Text en © 2016 Jia et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jia, Qi
Liu, Na
Xie, Ke
Dai, Yanwan
Han, Shaojie
Zhao, Xijuan
Qian, Lichao
Wang, Yunjing
Zhao, Jinping
Gorovits, Rena
Xie, Daoxin
Hong, Yiguo
Liu, Yule
CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana
title CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana
title_full CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana
title_fullStr CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana
title_full_unstemmed CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana
title_short CLCuMuB βC1 Subverts Ubiquitination by Interacting with NbSKP1s to Enhance Geminivirus Infection in Nicotiana benthamiana
title_sort clcumub βc1 subverts ubiquitination by interacting with nbskp1s to enhance geminivirus infection in nicotiana benthamiana
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912122/
https://www.ncbi.nlm.nih.gov/pubmed/27315204
http://dx.doi.org/10.1371/journal.ppat.1005668
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