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The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus

Casein kinases are serine/threonine protein kinases that are evolutionarily conserved in yeast and humans and are involved in a range of important cellular processes. However, the biological functions of casein kinases in the fungus Magnaporthe oryzae, the causal agent of destructive rice blast dise...

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Autores principales: Shi, Huan-Bin, Chen, Nan, Zhu, Xue-Ming, Su, Zhen-Zhu, Wang, Jiao-Yu, Lu, Jian-Ping, Liu, Xiao-Hong, Lin, Fu-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647852/
https://www.ncbi.nlm.nih.gov/pubmed/31392921
http://dx.doi.org/10.1080/21505594.2019.1649588
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author Shi, Huan-Bin
Chen, Nan
Zhu, Xue-Ming
Su, Zhen-Zhu
Wang, Jiao-Yu
Lu, Jian-Ping
Liu, Xiao-Hong
Lin, Fu-Cheng
author_facet Shi, Huan-Bin
Chen, Nan
Zhu, Xue-Ming
Su, Zhen-Zhu
Wang, Jiao-Yu
Lu, Jian-Ping
Liu, Xiao-Hong
Lin, Fu-Cheng
author_sort Shi, Huan-Bin
collection PubMed
description Casein kinases are serine/threonine protein kinases that are evolutionarily conserved in yeast and humans and are involved in a range of important cellular processes. However, the biological functions of casein kinases in the fungus Magnaporthe oryzae, the causal agent of destructive rice blast disease, are not characterized. Here, two casein kinases, MoYCK1 and MoHRR25, were identified and targeted for replacement, but only MoYCK1 was further characterized due to the possible nonviability of the MoHRR25 deletion mutant. Disruption of MoYCK1 caused pleiotropic defects in growth, conidiation, conidial germination, and appressorium formation and penetration, therefore resulting in reduced virulence in rice seedlings and barley leaves. Notably, the MoYCK1 deletion triggered quick lipidation of MoAtg8 and degradation of the autophagic marker protein GFP-MoAtg8 under nitrogen starvation conditions, in contrast to the wild type, indicating that autophagy activity was negatively regulated by MoYck1. Furthermore, we found that HOPS (homotypic fusion and vacuolar protein sorting) subunit MoVps41, a putative substrate of MoYck1, was co-located with MoAtg8 and positively required for the degradation of MoAtg8-PE and GFP-MoAtg8. In addition, MoYCK1 is also involved in the response to ionic hyperosmotic and heavy metal cation stresses. Taken together, our results revealed crucial roles of the casein kinase MoYck1 in regulating development, autophagy and virulence in M. oryzae.
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spelling pubmed-86478522021-12-07 The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus Shi, Huan-Bin Chen, Nan Zhu, Xue-Ming Su, Zhen-Zhu Wang, Jiao-Yu Lu, Jian-Ping Liu, Xiao-Hong Lin, Fu-Cheng Virulence Research Paper Casein kinases are serine/threonine protein kinases that are evolutionarily conserved in yeast and humans and are involved in a range of important cellular processes. However, the biological functions of casein kinases in the fungus Magnaporthe oryzae, the causal agent of destructive rice blast disease, are not characterized. Here, two casein kinases, MoYCK1 and MoHRR25, were identified and targeted for replacement, but only MoYCK1 was further characterized due to the possible nonviability of the MoHRR25 deletion mutant. Disruption of MoYCK1 caused pleiotropic defects in growth, conidiation, conidial germination, and appressorium formation and penetration, therefore resulting in reduced virulence in rice seedlings and barley leaves. Notably, the MoYCK1 deletion triggered quick lipidation of MoAtg8 and degradation of the autophagic marker protein GFP-MoAtg8 under nitrogen starvation conditions, in contrast to the wild type, indicating that autophagy activity was negatively regulated by MoYck1. Furthermore, we found that HOPS (homotypic fusion and vacuolar protein sorting) subunit MoVps41, a putative substrate of MoYck1, was co-located with MoAtg8 and positively required for the degradation of MoAtg8-PE and GFP-MoAtg8. In addition, MoYCK1 is also involved in the response to ionic hyperosmotic and heavy metal cation stresses. Taken together, our results revealed crucial roles of the casein kinase MoYck1 in regulating development, autophagy and virulence in M. oryzae. Taylor & Francis 2019-08-08 /pmc/articles/PMC8647852/ /pubmed/31392921 http://dx.doi.org/10.1080/21505594.2019.1649588 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Shi, Huan-Bin
Chen, Nan
Zhu, Xue-Ming
Su, Zhen-Zhu
Wang, Jiao-Yu
Lu, Jian-Ping
Liu, Xiao-Hong
Lin, Fu-Cheng
The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus
title The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus
title_full The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus
title_fullStr The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus
title_full_unstemmed The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus
title_short The casein kinase MoYck1 regulates development, autophagy, and virulence in the rice blast fungus
title_sort casein kinase moyck1 regulates development, autophagy, and virulence in the rice blast fungus
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647852/
https://www.ncbi.nlm.nih.gov/pubmed/31392921
http://dx.doi.org/10.1080/21505594.2019.1649588
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