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Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature

Natural environments require organisms to possess robust mechanisms allowing responses to seasonal trends. In Arabidopsis halleri, the flowering regulator AhgFLC shows upregulation and downregulation phases along with long-term past temperature, but the underlying machinery remains elusive. Here, we...

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Autores principales: Nishio, Haruki, Buzas, Diana M., Nagano, Atsushi J., Iwayama, Koji, Ushio, Masayuki, Kudoh, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195410/
https://www.ncbi.nlm.nih.gov/pubmed/32358518
http://dx.doi.org/10.1038/s41467-020-15896-4
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author Nishio, Haruki
Buzas, Diana M.
Nagano, Atsushi J.
Iwayama, Koji
Ushio, Masayuki
Kudoh, Hiroshi
author_facet Nishio, Haruki
Buzas, Diana M.
Nagano, Atsushi J.
Iwayama, Koji
Ushio, Masayuki
Kudoh, Hiroshi
author_sort Nishio, Haruki
collection PubMed
description Natural environments require organisms to possess robust mechanisms allowing responses to seasonal trends. In Arabidopsis halleri, the flowering regulator AhgFLC shows upregulation and downregulation phases along with long-term past temperature, but the underlying machinery remains elusive. Here, we investigate the seasonal dynamics of histone modifications, H3K27me3 and H3K4me3, at AhgFLC in a natural population. Our advanced modelling and transplant experiments reveal that H3K27me3-mediated chromatin regulation at AhgFLC provides two essential properties. One is the ability to respond to the long-term temperature trends via bidirectional interactions between H3K27me3 and H3K4me3; the other is the ratchet-like character of the AhgFLC system, i.e. reversible in the entire perennial life cycle but irreversible during the upregulation phase. Furthermore, we show that the long-term temperature trends are locally indexed at AhgFLC in the form of histone modifications. Our study provides a more comprehensive understanding of H3K27me3 function at AhgFLC in a complex natural environment.
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spelling pubmed-71954102020-05-05 Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature Nishio, Haruki Buzas, Diana M. Nagano, Atsushi J. Iwayama, Koji Ushio, Masayuki Kudoh, Hiroshi Nat Commun Article Natural environments require organisms to possess robust mechanisms allowing responses to seasonal trends. In Arabidopsis halleri, the flowering regulator AhgFLC shows upregulation and downregulation phases along with long-term past temperature, but the underlying machinery remains elusive. Here, we investigate the seasonal dynamics of histone modifications, H3K27me3 and H3K4me3, at AhgFLC in a natural population. Our advanced modelling and transplant experiments reveal that H3K27me3-mediated chromatin regulation at AhgFLC provides two essential properties. One is the ability to respond to the long-term temperature trends via bidirectional interactions between H3K27me3 and H3K4me3; the other is the ratchet-like character of the AhgFLC system, i.e. reversible in the entire perennial life cycle but irreversible during the upregulation phase. Furthermore, we show that the long-term temperature trends are locally indexed at AhgFLC in the form of histone modifications. Our study provides a more comprehensive understanding of H3K27me3 function at AhgFLC in a complex natural environment. Nature Publishing Group UK 2020-05-01 /pmc/articles/PMC7195410/ /pubmed/32358518 http://dx.doi.org/10.1038/s41467-020-15896-4 Text en © The Author(s) 2020 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/.
spellingShingle Article
Nishio, Haruki
Buzas, Diana M.
Nagano, Atsushi J.
Iwayama, Koji
Ushio, Masayuki
Kudoh, Hiroshi
Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
title Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
title_full Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
title_fullStr Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
title_full_unstemmed Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
title_short Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
title_sort repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195410/
https://www.ncbi.nlm.nih.gov/pubmed/32358518
http://dx.doi.org/10.1038/s41467-020-15896-4
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