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3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize
BACKGROUND: Maize ears and tassels are two separate types of inflorescence which are initiated by similar developmental processes but gradually develop distinct architectures. However, coordinated trans and cis regulation of differentially expressed genes determining ear and tassel architecture with...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296987/ https://www.ncbi.nlm.nih.gov/pubmed/32546248 http://dx.doi.org/10.1186/s13059-020-02063-7 |
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author | Sun, Yonghao Dong, Liang Zhang, Ying Lin, Da Xu, Weize Ke, Changxiong Han, Linqian Deng, Lulu Li, Guoliang Jackson, David Li, Xingwang Yang, Fang |
author_facet | Sun, Yonghao Dong, Liang Zhang, Ying Lin, Da Xu, Weize Ke, Changxiong Han, Linqian Deng, Lulu Li, Guoliang Jackson, David Li, Xingwang Yang, Fang |
author_sort | Sun, Yonghao |
collection | PubMed |
description | BACKGROUND: Maize ears and tassels are two separate types of inflorescence which are initiated by similar developmental processes but gradually develop distinct architectures. However, coordinated trans and cis regulation of differentially expressed genes determining ear and tassel architecture within the 3D genome context is largely unknown. RESULTS: We identify 56,055 and 52,633 open chromatin regions (OCRs) in developing maize ear and tassel primordia using ATAC-seq and characterize combinatorial epigenome features around these OCRs using ChIP-seq, Bisulfite-seq, and RNA-seq datasets. Our integrative analysis of coordinated epigenetic modification and transcription factor binding to OCRs highlights the cis and trans regulation of differentially expressed genes in ear and tassel controlling inflorescence architecture. We further systematically map chromatin interactions at high-resolution in corresponding tissues using in situ digestion-ligation-only Hi-C (DLO Hi-C). The extensive chromatin loops connecting OCRs and genes provide a 3D view on cis- and trans-regulatory modules responsible for ear- and tassel-specific gene expression. We find that intergenic SNPs tend to locate in distal OCRs, and our chromatin interaction maps provide a potential mechanism for trait-associated intergenic SNPs that may contribute to phenotypic variation by influencing target gene expression through chromatin loops. CONCLUSIONS: Our comprehensive epigenome annotations and 3D genome maps serve as valuable resource and provide a deep understanding of the complex regulatory mechanisms of genes underlying developmental and morphological diversities between maize ear and tassel. |
format | Online Article Text |
id | pubmed-7296987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72969872020-06-17 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize Sun, Yonghao Dong, Liang Zhang, Ying Lin, Da Xu, Weize Ke, Changxiong Han, Linqian Deng, Lulu Li, Guoliang Jackson, David Li, Xingwang Yang, Fang Genome Biol Research BACKGROUND: Maize ears and tassels are two separate types of inflorescence which are initiated by similar developmental processes but gradually develop distinct architectures. However, coordinated trans and cis regulation of differentially expressed genes determining ear and tassel architecture within the 3D genome context is largely unknown. RESULTS: We identify 56,055 and 52,633 open chromatin regions (OCRs) in developing maize ear and tassel primordia using ATAC-seq and characterize combinatorial epigenome features around these OCRs using ChIP-seq, Bisulfite-seq, and RNA-seq datasets. Our integrative analysis of coordinated epigenetic modification and transcription factor binding to OCRs highlights the cis and trans regulation of differentially expressed genes in ear and tassel controlling inflorescence architecture. We further systematically map chromatin interactions at high-resolution in corresponding tissues using in situ digestion-ligation-only Hi-C (DLO Hi-C). The extensive chromatin loops connecting OCRs and genes provide a 3D view on cis- and trans-regulatory modules responsible for ear- and tassel-specific gene expression. We find that intergenic SNPs tend to locate in distal OCRs, and our chromatin interaction maps provide a potential mechanism for trait-associated intergenic SNPs that may contribute to phenotypic variation by influencing target gene expression through chromatin loops. CONCLUSIONS: Our comprehensive epigenome annotations and 3D genome maps serve as valuable resource and provide a deep understanding of the complex regulatory mechanisms of genes underlying developmental and morphological diversities between maize ear and tassel. BioMed Central 2020-06-16 /pmc/articles/PMC7296987/ /pubmed/32546248 http://dx.doi.org/10.1186/s13059-020-02063-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Sun, Yonghao Dong, Liang Zhang, Ying Lin, Da Xu, Weize Ke, Changxiong Han, Linqian Deng, Lulu Li, Guoliang Jackson, David Li, Xingwang Yang, Fang 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
title | 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
title_full | 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
title_fullStr | 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
title_full_unstemmed | 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
title_short | 3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
title_sort | 3d genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296987/ https://www.ncbi.nlm.nih.gov/pubmed/32546248 http://dx.doi.org/10.1186/s13059-020-02063-7 |
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