Type I J-domain NbMIP1 proteins are required for both Tobacco mosaic virus infection and plant innate immunity

Tm-2² is a coiled coil-nucleotide binding-leucine rich repeat resistance protein that confers durable extreme resistance against Tomato mosaic virus (ToMV) and Tobacco mosaic virus (TMV) by recognizing the viral movement protein (MP). Here we report that the Nicotiana benthamiana J-domain MIP1 prote...

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Veröffentlicht in:PLoS pathogens 2013-10, Vol.9 (10), p.e1003659-e1003659
Hauptverfasser: Du, Yumei, Zhao, Jinping, Chen, Tianyuan, Liu, Qi, Zhang, Haili, Wang, Yan, Hong, Yiguo, Xiao, Fangming, Zhang, Ling, Shen, Qianhua, Liu, Yule
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container_issue 10
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container_title PLoS pathogens
container_volume 9
creator Du, Yumei
Zhao, Jinping
Chen, Tianyuan
Liu, Qi
Zhang, Haili
Wang, Yan
Hong, Yiguo
Xiao, Fangming
Zhang, Ling
Shen, Qianhua
Liu, Yule
description Tm-2² is a coiled coil-nucleotide binding-leucine rich repeat resistance protein that confers durable extreme resistance against Tomato mosaic virus (ToMV) and Tobacco mosaic virus (TMV) by recognizing the viral movement protein (MP). Here we report that the Nicotiana benthamiana J-domain MIP1 proteins (NbMIP1s) associate with tobamovirus MP, Tm-2² and SGT1. Silencing of NbMIP1s reduced TMV movement and compromised Tm-2²-mediated resistance against TMV and ToMV. Furthermore, silencing of NbMIP1s reduced the steady-state protein levels of ToMV MP and Tm-2². Moreover, NbMIP1s are required for plant resistance induced by other R genes and the nonhost pathogen Pseudomonas syringae pv. tomato (Pst) DC3000. In addition, we found that SGT1 associates with Tm-2² and is required for Tm-2²-mediated resistance against TMV. These results suggest that NbMIP1s function as co-chaperones during virus infection and plant immunity.
doi_str_mv 10.1371/journal.ppat.1003659
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Here we report that the Nicotiana benthamiana J-domain MIP1 proteins (NbMIP1s) associate with tobamovirus MP, Tm-2² and SGT1. Silencing of NbMIP1s reduced TMV movement and compromised Tm-2²-mediated resistance against TMV and ToMV. Furthermore, silencing of NbMIP1s reduced the steady-state protein levels of ToMV MP and Tm-2². Moreover, NbMIP1s are required for plant resistance induced by other R genes and the nonhost pathogen Pseudomonas syringae pv. tomato (Pst) DC3000. In addition, we found that SGT1 associates with Tm-2² and is required for Tm-2²-mediated resistance against TMV. These results suggest that NbMIP1s function as co-chaperones during virus infection and plant immunity.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24098120</pmid><doi>10.1371/journal.ppat.1003659</doi><oa>free_for_read</oa></addata></record>
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subjects Apoptosis
Disease Resistance - genetics
Disease Resistance - immunology
Experiments
Glucosyltransferases - genetics
Glucosyltransferases - immunology
Health aspects
Host-parasite relationships
Infections
Leaves
Molecular Chaperones - genetics
Molecular Chaperones - immunology
Nicotiana - genetics
Nicotiana - immunology
Nicotiana - virology
Physiological aspects
Plant defenses
Plant Diseases - genetics
Plant Diseases - immunology
Plant Diseases - virology
Plant Proteins - genetics
Plant Proteins - immunology
Protein folding
Protein Structure, Tertiary
Pseudomonas syringae
Tobacco
Tobacco mosaic virus
Tobacco Mosaic Virus - genetics
Tobacco Mosaic Virus - immunology
Viral infections
Viral proteins
title Type I J-domain NbMIP1 proteins are required for both Tobacco mosaic virus infection and plant innate immunity
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