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H3K4me2 functions as a repressive epigenetic mark in plants
BACKGROUND: In animals, H3K4me2 and H3K4me3 are enriched at the transcription start site (TSS) and function as epigenetic marks that regulate gene transcription, but their functions in plants have not been fully characterized. RESULTS: We used chromatin immunoprecipitation sequencing to analyze the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604379/ https://www.ncbi.nlm.nih.gov/pubmed/31266517 http://dx.doi.org/10.1186/s13072-019-0285-6 |
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author | Liu, Yuhao Liu, Kunpeng Yin, Liufan Yu, Yu Qi, Ji Shen, Wen-Hui Zhu, Jun Zhang, Yijing Dong, Aiwu |
author_facet | Liu, Yuhao Liu, Kunpeng Yin, Liufan Yu, Yu Qi, Ji Shen, Wen-Hui Zhu, Jun Zhang, Yijing Dong, Aiwu |
author_sort | Liu, Yuhao |
collection | PubMed |
description | BACKGROUND: In animals, H3K4me2 and H3K4me3 are enriched at the transcription start site (TSS) and function as epigenetic marks that regulate gene transcription, but their functions in plants have not been fully characterized. RESULTS: We used chromatin immunoprecipitation sequencing to analyze the rice genome-wide changes to H3K4me1/H3K4me2/H3K4me3 following the loss of an H3K4-specific methyltransferase, SDG701. The knockdown of SDG701 resulted in a global decrease in H3K4me2/H3K4me3 levels throughout the rice genome. An RNA-sequencing analysis revealed that many genes related to diverse developmental processes were misregulated in the SDG701 knockdown mutant. In rice, H3K4me3 and H3K36me3 are positively correlated with gene transcription; however, surprisingly, the H3K4me2 level was negatively associated with gene transcription levels. Furthermore, the H3K4me3 level at the TSS region decreased significantly in the genes that exhibited down-regulated expression in the SDG701 knockdown mutant. In contrast, the genes with up-regulated expression in the mutant were associated with a considerable decrease in H3K4me2 levels over the gene body region. CONCLUSION: A comparison of the genome-wide distributions of H3K4me2 in eukaryotes indicated that the H3K4me2 level is not correlated with the gene transcription level in yeast, but is positively and negatively correlated with gene expression in animals and plants, respectively. Our results uncovered H3K4me2 as a novel repressive mark in plants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-019-0285-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6604379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66043792019-07-12 H3K4me2 functions as a repressive epigenetic mark in plants Liu, Yuhao Liu, Kunpeng Yin, Liufan Yu, Yu Qi, Ji Shen, Wen-Hui Zhu, Jun Zhang, Yijing Dong, Aiwu Epigenetics Chromatin Research BACKGROUND: In animals, H3K4me2 and H3K4me3 are enriched at the transcription start site (TSS) and function as epigenetic marks that regulate gene transcription, but their functions in plants have not been fully characterized. RESULTS: We used chromatin immunoprecipitation sequencing to analyze the rice genome-wide changes to H3K4me1/H3K4me2/H3K4me3 following the loss of an H3K4-specific methyltransferase, SDG701. The knockdown of SDG701 resulted in a global decrease in H3K4me2/H3K4me3 levels throughout the rice genome. An RNA-sequencing analysis revealed that many genes related to diverse developmental processes were misregulated in the SDG701 knockdown mutant. In rice, H3K4me3 and H3K36me3 are positively correlated with gene transcription; however, surprisingly, the H3K4me2 level was negatively associated with gene transcription levels. Furthermore, the H3K4me3 level at the TSS region decreased significantly in the genes that exhibited down-regulated expression in the SDG701 knockdown mutant. In contrast, the genes with up-regulated expression in the mutant were associated with a considerable decrease in H3K4me2 levels over the gene body region. CONCLUSION: A comparison of the genome-wide distributions of H3K4me2 in eukaryotes indicated that the H3K4me2 level is not correlated with the gene transcription level in yeast, but is positively and negatively correlated with gene expression in animals and plants, respectively. Our results uncovered H3K4me2 as a novel repressive mark in plants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-019-0285-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-02 /pmc/articles/PMC6604379/ /pubmed/31266517 http://dx.doi.org/10.1186/s13072-019-0285-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Liu, Yuhao Liu, Kunpeng Yin, Liufan Yu, Yu Qi, Ji Shen, Wen-Hui Zhu, Jun Zhang, Yijing Dong, Aiwu H3K4me2 functions as a repressive epigenetic mark in plants |
title | H3K4me2 functions as a repressive epigenetic mark in plants |
title_full | H3K4me2 functions as a repressive epigenetic mark in plants |
title_fullStr | H3K4me2 functions as a repressive epigenetic mark in plants |
title_full_unstemmed | H3K4me2 functions as a repressive epigenetic mark in plants |
title_short | H3K4me2 functions as a repressive epigenetic mark in plants |
title_sort | h3k4me2 functions as a repressive epigenetic mark in plants |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604379/ https://www.ncbi.nlm.nih.gov/pubmed/31266517 http://dx.doi.org/10.1186/s13072-019-0285-6 |
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