Cargando…

Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran

Plant cells enhance the tolerances to abiotic and biotic stresses via recognition of the stress, activation and nuclear import of signaling factors, up-regulation of defense genes, nuclear export of mRNA and translation of defense proteins. Nuclear pore-mediated transports should play critical roles...

Descripción completa

Detalles Bibliográficos
Autores principales: Mizuno, Yuri, Ohtsu, Mina, Shibata, Yusuke, Tanaka, Aiko, Camagna, Maurizio, Ojika, Makoto, Mori, Hitoshi, Sato, Ikuo, Chiba, Sotaro, Kawakita, Kazuhito, Takemoto, Daigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418045/
https://www.ncbi.nlm.nih.gov/pubmed/30906303
http://dx.doi.org/10.3389/fpls.2019.00222
_version_ 1783403649710424064
author Mizuno, Yuri
Ohtsu, Mina
Shibata, Yusuke
Tanaka, Aiko
Camagna, Maurizio
Ojika, Makoto
Mori, Hitoshi
Sato, Ikuo
Chiba, Sotaro
Kawakita, Kazuhito
Takemoto, Daigo
author_facet Mizuno, Yuri
Ohtsu, Mina
Shibata, Yusuke
Tanaka, Aiko
Camagna, Maurizio
Ojika, Makoto
Mori, Hitoshi
Sato, Ikuo
Chiba, Sotaro
Kawakita, Kazuhito
Takemoto, Daigo
author_sort Mizuno, Yuri
collection PubMed
description Plant cells enhance the tolerances to abiotic and biotic stresses via recognition of the stress, activation and nuclear import of signaling factors, up-regulation of defense genes, nuclear export of mRNA and translation of defense proteins. Nuclear pore-mediated transports should play critical roles in these processes, however, the regulatory mechanisms of nuclear-cytoplasmic transport during stress responses are largely unknown. In this study, a regulator of nuclear export of RNA and proteins, NbRanBP1-1 (Ran-binding protein1-1), was identified as an essential gene for the resistance of Nicotiana benthamiana to potato blight pathogen Phytophthora infestans. NbRanBP1-1-silenced plants showed delayed accumulation of capsidiol, a sesquiterpenoid phytoalexin, in response to elicitor treatment, and reduced resistance to P. infestans. Abnormal accumulation of mRNA was observed in NbRanBP1-1-silenced plants, indicating that NbRanBP1-1 is involved in the nuclear export of mRNA. In NbRanBP1-1-silenced plants, elicitor-induced expression of defense genes, NbEAS and NbWIPK, was not affected in the early stage of defense induction, but the accumulation of NbWIPK protein was reduced. Nuclear export of the small G-protein NbRan1a was activated during the induction of plant defense, whereas this process was compromised in NbRanBP1-1-silenced plants. Silencing of genes encoding the nuclear pore proteins, Nup75 and Nup160, also caused abnormal nuclear accumulation of mRNA, defects in the nuclear export of NbRan1a, and reduced production of capsidiol, resulting in decreased resistance to P. infestans. These results suggest that nuclear export of NbRan is a key event for defense induction in N. benthamiana, and both RanBP1-1 and nucleoporins play important roles in the process.
format Online
Article
Text
id pubmed-6418045
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-64180452019-03-22 Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran Mizuno, Yuri Ohtsu, Mina Shibata, Yusuke Tanaka, Aiko Camagna, Maurizio Ojika, Makoto Mori, Hitoshi Sato, Ikuo Chiba, Sotaro Kawakita, Kazuhito Takemoto, Daigo Front Plant Sci Plant Science Plant cells enhance the tolerances to abiotic and biotic stresses via recognition of the stress, activation and nuclear import of signaling factors, up-regulation of defense genes, nuclear export of mRNA and translation of defense proteins. Nuclear pore-mediated transports should play critical roles in these processes, however, the regulatory mechanisms of nuclear-cytoplasmic transport during stress responses are largely unknown. In this study, a regulator of nuclear export of RNA and proteins, NbRanBP1-1 (Ran-binding protein1-1), was identified as an essential gene for the resistance of Nicotiana benthamiana to potato blight pathogen Phytophthora infestans. NbRanBP1-1-silenced plants showed delayed accumulation of capsidiol, a sesquiterpenoid phytoalexin, in response to elicitor treatment, and reduced resistance to P. infestans. Abnormal accumulation of mRNA was observed in NbRanBP1-1-silenced plants, indicating that NbRanBP1-1 is involved in the nuclear export of mRNA. In NbRanBP1-1-silenced plants, elicitor-induced expression of defense genes, NbEAS and NbWIPK, was not affected in the early stage of defense induction, but the accumulation of NbWIPK protein was reduced. Nuclear export of the small G-protein NbRan1a was activated during the induction of plant defense, whereas this process was compromised in NbRanBP1-1-silenced plants. Silencing of genes encoding the nuclear pore proteins, Nup75 and Nup160, also caused abnormal nuclear accumulation of mRNA, defects in the nuclear export of NbRan1a, and reduced production of capsidiol, resulting in decreased resistance to P. infestans. These results suggest that nuclear export of NbRan is a key event for defense induction in N. benthamiana, and both RanBP1-1 and nucleoporins play important roles in the process. Frontiers Media S.A. 2019-03-08 /pmc/articles/PMC6418045/ /pubmed/30906303 http://dx.doi.org/10.3389/fpls.2019.00222 Text en Copyright © 2019 Mizuno, Ohtsu, Shibata, Tanaka, Camagna, Ojika, Mori, Sato, Chiba, Kawakita and Takemoto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Mizuno, Yuri
Ohtsu, Mina
Shibata, Yusuke
Tanaka, Aiko
Camagna, Maurizio
Ojika, Makoto
Mori, Hitoshi
Sato, Ikuo
Chiba, Sotaro
Kawakita, Kazuhito
Takemoto, Daigo
Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran
title Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran
title_full Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran
title_fullStr Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran
title_full_unstemmed Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran
title_short Nicotiana benthamiana RanBP1-1 Is Involved in the Induction of Disease Resistance via Regulation of Nuclear-Cytoplasmic Transport of Small GTPase Ran
title_sort nicotiana benthamiana ranbp1-1 is involved in the induction of disease resistance via regulation of nuclear-cytoplasmic transport of small gtpase ran
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418045/
https://www.ncbi.nlm.nih.gov/pubmed/30906303
http://dx.doi.org/10.3389/fpls.2019.00222
work_keys_str_mv AT mizunoyuri nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT ohtsumina nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT shibatayusuke nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT tanakaaiko nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT camagnamaurizio nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT ojikamakoto nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT morihitoshi nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT satoikuo nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT chibasotaro nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT kawakitakazuhito nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran
AT takemotodaigo nicotianabenthamianaranbp11isinvolvedintheinductionofdiseaseresistanceviaregulationofnuclearcytoplasmictransportofsmallgtpaseran