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Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes
BACKGROUND: Our understanding of how the complexity of the wheat genome influences the distribution of chromatin states along the homoeologous chromosomes is limited. Using a differential nuclease sensitivity assay, we investigate the chromatin states of the coding and repetitive regions of the allo...
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/PMC7368981/ https://www.ncbi.nlm.nih.gov/pubmed/32684157 http://dx.doi.org/10.1186/s13059-020-02093-1 |
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author | Jordan, Katherine W. He, Fei de Soto, Monica Fernandez Akhunova, Alina Akhunov, Eduard |
author_facet | Jordan, Katherine W. He, Fei de Soto, Monica Fernandez Akhunova, Alina Akhunov, Eduard |
author_sort | Jordan, Katherine W. |
collection | PubMed |
description | BACKGROUND: Our understanding of how the complexity of the wheat genome influences the distribution of chromatin states along the homoeologous chromosomes is limited. Using a differential nuclease sensitivity assay, we investigate the chromatin states of the coding and repetitive regions of the allopolyploid wheat genome. RESULTS: Although open chromatin is found to be significantly enriched around genes, the majority of MNase-sensitive regions are located within transposable elements (TEs). Chromatin of the smaller D genome is more accessible than that of the larger A and B genomes. Chromatin states of different TEs vary among families and are influenced by the TEs’ chromosomal position and proximity to genes. While the chromatin accessibility of genes is influenced by proximity to TEs, and not by their position on the chromosomes, we observe a negative chromatin accessibility gradient along the telomere-centromere axis in the intergenic regions, positively correlated with the distance between genes. Both gene expression levels and homoeologous gene expression bias are correlated with chromatin accessibility in promoter regions. The differential nuclease sensitivity assay accurately predicts previously detected centromere locations. SNPs located within more accessible chromatin explain a higher proportion of genetic variance for a number of agronomic traits than SNPs located within more closed chromatin. CONCLUSIONS: Chromatin states in the wheat genome are shaped by the interplay of repetitive and gene-encoding regions that are predictive of the functional and structural organization of chromosomes, providing a powerful framework for detecting genomic features involved in gene regulation and prioritizing genomic variation to explain phenotypes. |
format | Online Article Text |
id | pubmed-7368981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73689812020-07-21 Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes Jordan, Katherine W. He, Fei de Soto, Monica Fernandez Akhunova, Alina Akhunov, Eduard Genome Biol Research BACKGROUND: Our understanding of how the complexity of the wheat genome influences the distribution of chromatin states along the homoeologous chromosomes is limited. Using a differential nuclease sensitivity assay, we investigate the chromatin states of the coding and repetitive regions of the allopolyploid wheat genome. RESULTS: Although open chromatin is found to be significantly enriched around genes, the majority of MNase-sensitive regions are located within transposable elements (TEs). Chromatin of the smaller D genome is more accessible than that of the larger A and B genomes. Chromatin states of different TEs vary among families and are influenced by the TEs’ chromosomal position and proximity to genes. While the chromatin accessibility of genes is influenced by proximity to TEs, and not by their position on the chromosomes, we observe a negative chromatin accessibility gradient along the telomere-centromere axis in the intergenic regions, positively correlated with the distance between genes. Both gene expression levels and homoeologous gene expression bias are correlated with chromatin accessibility in promoter regions. The differential nuclease sensitivity assay accurately predicts previously detected centromere locations. SNPs located within more accessible chromatin explain a higher proportion of genetic variance for a number of agronomic traits than SNPs located within more closed chromatin. CONCLUSIONS: Chromatin states in the wheat genome are shaped by the interplay of repetitive and gene-encoding regions that are predictive of the functional and structural organization of chromosomes, providing a powerful framework for detecting genomic features involved in gene regulation and prioritizing genomic variation to explain phenotypes. BioMed Central 2020-07-19 /pmc/articles/PMC7368981/ /pubmed/32684157 http://dx.doi.org/10.1186/s13059-020-02093-1 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 Jordan, Katherine W. He, Fei de Soto, Monica Fernandez Akhunova, Alina Akhunov, Eduard Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
title | Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
title_full | Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
title_fullStr | Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
title_full_unstemmed | Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
title_short | Differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
title_sort | differential chromatin accessibility landscape reveals structural and functional features of the allopolyploid wheat chromosomes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368981/ https://www.ncbi.nlm.nih.gov/pubmed/32684157 http://dx.doi.org/10.1186/s13059-020-02093-1 |
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