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

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          Abstract

          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.

          Abstract

          Our study shows that post-translational modification of histones is essential for regulating the biosynthesis and emission of floral scent compounds, thus providing insights into the regulation of secondary metabolism at chromatin level.

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          Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

          In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate numbers, discreteness, large dynamic range and the presence of outliers require a suitable statistical approach. We present DESeq2, a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. This enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression. The DESeq2 package is available at http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html. Electronic supplementary material The online version of this article (doi:10.1186/s13059-014-0550-8) contains supplementary material, which is available to authorized users.
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            Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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              Fast gapped-read alignment with Bowtie 2.

              As the rate of sequencing increases, greater throughput is demanded from read aligners. The full-text minute index is often used to make alignment very fast and memory-efficient, but the approach is ill-suited to finding longer, gapped alignments. Bowtie 2 combines the strengths of the full-text minute index with the flexibility and speed of hardware-accelerated dynamic programming algorithms to achieve a combination of high speed, sensitivity and accuracy.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                J Exp Bot
                J Exp Bot
                exbotj
                Journal of Experimental Botany
                Oxford University Press (UK )
                0022-0957
                1460-2431
                04 May 2021
                19 February 2021
                19 February 2021
                : 72
                : 10
                : 3704-3722
                Affiliations
                [1 ] Department of Horticulture and Landscape Architecture, Purdue University , West Lafayette, IN 47907,USA
                [2 ] Purdue Center for Plant Biology, Purdue University , West Lafayette, IN 47907,USA
                [3 ] Department of Biochemistry, Purdue University , West Lafayette, IN 47907,USA
                [4 ] Oklahoma State University , USA
                Author notes
                Author information
                https://orcid.org/0000-0002-5258-7355
                Article
                erab072
                10.1093/jxb/erab072
                8096599
                33606881
                133d5c07-abc2-4ef5-9f52-56d592b1876f
                © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Experimental Biology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 October 2020
                : 09 February 2021
                : 15 February 2021
                : 01 April 2021
                Page count
                Pages: 19
                Funding
                Funded by: USDA National Institute of Food and Agriculture;
                Award ID: 1013620
                Award ID: 177845
                Award ID: 2019-67012-29660
                Categories
                Research Papers
                Photosynthesis and Metabolism
                AcademicSubjects/SCI01210

                Plant science & Botany
                epigenome,floral volatile,histone acetylation,organic compounds,secondary metabolites

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