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A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs

Plant immunity frequently incurs growth penalties, which known as the trade-off between immunity and growth. Heterosis, the phenotypic superiority of a hybrid over its parents, has been demonstrated for many traits but rarely for disease resistance. Here, we report that the central circadian oscilla...

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Autores principales: Yang, Li, Liu, Pengtao, Wang, Xuncheng, Jia, Aolin, Ren, Diqiu, Tang, Yaru, Tang, Yaqi, Deng, Xing Wang, He, Guangming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055661/
https://www.ncbi.nlm.nih.gov/pubmed/33875651
http://dx.doi.org/10.1038/s41467-021-22268-z
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author Yang, Li
Liu, Pengtao
Wang, Xuncheng
Jia, Aolin
Ren, Diqiu
Tang, Yaru
Tang, Yaqi
Deng, Xing Wang
He, Guangming
author_facet Yang, Li
Liu, Pengtao
Wang, Xuncheng
Jia, Aolin
Ren, Diqiu
Tang, Yaru
Tang, Yaqi
Deng, Xing Wang
He, Guangming
author_sort Yang, Li
collection PubMed
description Plant immunity frequently incurs growth penalties, which known as the trade-off between immunity and growth. Heterosis, the phenotypic superiority of a hybrid over its parents, has been demonstrated for many traits but rarely for disease resistance. Here, we report that the central circadian oscillator, CCA1, confers heterosis for bacterial defense in hybrids without growth vigor costs, and it even significantly enhances the growth heterosis of hybrids under pathogen infection. The genetic perturbation of CCA1 abrogated heterosis for both defense and growth in hybrids. Upon pathogen attack, the expression of CCA1 in F(1) hybrids is precisely modulated at different time points during the day by its rhythmic histone modifications. Before dawn of the first infection day, epigenetic activation of CCA1 promotes an elevation of salicylic acid accumulation in hybrids, enabling heterosis for defense. During the middle of every infection day, diurnal epigenetic repression of CCA1 leads to rhythmically increased chlorophyll synthesis and starch metabolism in hybrids, effectively eliminating the immunity-growth heterosis trade-offs in hybrids.
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spelling pubmed-80556612021-05-11 A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs Yang, Li Liu, Pengtao Wang, Xuncheng Jia, Aolin Ren, Diqiu Tang, Yaru Tang, Yaqi Deng, Xing Wang He, Guangming Nat Commun Article Plant immunity frequently incurs growth penalties, which known as the trade-off between immunity and growth. Heterosis, the phenotypic superiority of a hybrid over its parents, has been demonstrated for many traits but rarely for disease resistance. Here, we report that the central circadian oscillator, CCA1, confers heterosis for bacterial defense in hybrids without growth vigor costs, and it even significantly enhances the growth heterosis of hybrids under pathogen infection. The genetic perturbation of CCA1 abrogated heterosis for both defense and growth in hybrids. Upon pathogen attack, the expression of CCA1 in F(1) hybrids is precisely modulated at different time points during the day by its rhythmic histone modifications. Before dawn of the first infection day, epigenetic activation of CCA1 promotes an elevation of salicylic acid accumulation in hybrids, enabling heterosis for defense. During the middle of every infection day, diurnal epigenetic repression of CCA1 leads to rhythmically increased chlorophyll synthesis and starch metabolism in hybrids, effectively eliminating the immunity-growth heterosis trade-offs in hybrids. Nature Publishing Group UK 2021-04-19 /pmc/articles/PMC8055661/ /pubmed/33875651 http://dx.doi.org/10.1038/s41467-021-22268-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yang, Li
Liu, Pengtao
Wang, Xuncheng
Jia, Aolin
Ren, Diqiu
Tang, Yaru
Tang, Yaqi
Deng, Xing Wang
He, Guangming
A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
title A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
title_full A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
title_fullStr A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
title_full_unstemmed A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
title_short A central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
title_sort central circadian oscillator confers defense heterosis in hybrids without growth vigor costs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055661/
https://www.ncbi.nlm.nih.gov/pubmed/33875651
http://dx.doi.org/10.1038/s41467-021-22268-z
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