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Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers

Biosynthesis of secondary metabolites relies on primary metabolic pathways to provide precursors, energy, and cofactors, thus requiring coordinated regulation of primary and secondary metabolic networks. However, to date, it remains largely unknown how this coordination is achieved. Using Petunia hy...

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Autores principales: Patrick, Ryan M, Huang, Xing-Qi, Dudareva, Natalia, Li, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096599/
https://www.ncbi.nlm.nih.gov/pubmed/33606881
http://dx.doi.org/10.1093/jxb/erab072
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author Patrick, Ryan M
Huang, Xing-Qi
Dudareva, Natalia
Li, Ying
author_facet Patrick, Ryan M
Huang, Xing-Qi
Dudareva, Natalia
Li, Ying
author_sort Patrick, Ryan M
collection PubMed
description Biosynthesis of secondary metabolites relies on primary metabolic pathways to provide precursors, energy, and cofactors, thus requiring coordinated regulation of primary and secondary metabolic networks. However, to date, it remains largely unknown how this coordination is achieved. Using Petunia hybrida flowers, which emit high levels of phenylpropanoid/benzenoid volatile organic compounds (VOCs), we uncovered genome-wide dynamic deposition of histone H3 lysine 9 acetylation (H3K9ac) during anthesis as an underlying mechanism to coordinate primary and secondary metabolic networks. The observed epigenome reprogramming is accompanied by transcriptional activation at gene loci involved in primary metabolic pathways that provide precursor phenylalanine, as well as secondary metabolic pathways to produce volatile compounds. We also observed transcriptional repression among genes involved in alternative phenylpropanoid branches that compete for metabolic precursors. We show that GNAT family histone acetyltransferase(s) (HATs) are required for the expression of genes involved in VOC biosynthesis and emission, by using chemical inhibitors of HATs, and by knocking down a specific HAT gene, ELP3, through transient RNAi. Together, our study supports that regulatory mechanisms at chromatin level may play an essential role in activating primary and secondary metabolic pathways to regulate VOC synthesis in petunia flowers.
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spelling pubmed-80965992021-05-10 Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers Patrick, Ryan M Huang, Xing-Qi Dudareva, Natalia Li, Ying J Exp Bot Research Papers Biosynthesis of secondary metabolites relies on primary metabolic pathways to provide precursors, energy, and cofactors, thus requiring coordinated regulation of primary and secondary metabolic networks. However, to date, it remains largely unknown how this coordination is achieved. Using Petunia hybrida flowers, which emit high levels of phenylpropanoid/benzenoid volatile organic compounds (VOCs), we uncovered genome-wide dynamic deposition of histone H3 lysine 9 acetylation (H3K9ac) during anthesis as an underlying mechanism to coordinate primary and secondary metabolic networks. The observed epigenome reprogramming is accompanied by transcriptional activation at gene loci involved in primary metabolic pathways that provide precursor phenylalanine, as well as secondary metabolic pathways to produce volatile compounds. We also observed transcriptional repression among genes involved in alternative phenylpropanoid branches that compete for metabolic precursors. We show that GNAT family histone acetyltransferase(s) (HATs) are required for the expression of genes involved in VOC biosynthesis and emission, by using chemical inhibitors of HATs, and by knocking down a specific HAT gene, ELP3, through transient RNAi. Together, our study supports that regulatory mechanisms at chromatin level may play an essential role in activating primary and secondary metabolic pathways to regulate VOC synthesis in petunia flowers. Oxford University Press 2021-02-19 /pmc/articles/PMC8096599/ /pubmed/33606881 http://dx.doi.org/10.1093/jxb/erab072 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Patrick, Ryan M
Huang, Xing-Qi
Dudareva, Natalia
Li, Ying
Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
title Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
title_full Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
title_fullStr Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
title_full_unstemmed Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
title_short Dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
title_sort dynamic histone acetylation in floral volatile synthesis and emission in petunia flowers
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096599/
https://www.ncbi.nlm.nih.gov/pubmed/33606881
http://dx.doi.org/10.1093/jxb/erab072
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