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A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits

BACKGROUND: Covalent modifications of histones and histone variants have great influence on chromatin structure, which is involved in the transcriptional regulation of gene expression. Chromatin immunoprecipitation (ChIP) is a powerful tool for studying in vivo DNA-histone interactions. Strawberry i...

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Autores principales: Huang, Xiaorong, Pan, Qinwei, Lin, Ying, Gu, Tingting, Li, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998251/
https://www.ncbi.nlm.nih.gov/pubmed/32025237
http://dx.doi.org/10.1186/s13007-020-0556-z
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author Huang, Xiaorong
Pan, Qinwei
Lin, Ying
Gu, Tingting
Li, Yi
author_facet Huang, Xiaorong
Pan, Qinwei
Lin, Ying
Gu, Tingting
Li, Yi
author_sort Huang, Xiaorong
collection PubMed
description BACKGROUND: Covalent modifications of histones and histone variants have great influence on chromatin structure, which is involved in the transcriptional regulation of gene expression. Chromatin immunoprecipitation (ChIP) is a powerful tool for studying in vivo DNA-histone interactions. Strawberry is a model for Rosaceae and non-climacteric fruits, in which histone modifications have been implicated to affect fruit development and ripening. However, a validated ChIP method has not been reported in strawberry, probably due to its high levels of polysaccharides which affect the quality of prepared chromatin and the efficiency of immunoprecipitation. RESULTS: We describe a native chromatin immunoprecipitation (N-ChIP) protocol suitable for strawberry by optimizing the parameters for nuclei isolation, chromatin extraction, DNA fragmentation and validation analysis using quantitative real-time PCR (qRT-PCR). The qRT-PCR results show that both the active mark H3K36me3 and the silent mark H3K9me2 are efficiently immunoprecipitated for the enriched regions. Compared to X-ChIP (cross-linked chromatin followed by immunoprecipitation), our optimized N-ChIP procedure has a higher signal-to-noise ratio and a lower background for both the active and the silent histone modifications. Furthermore, high-throughput sequencing following N-ChIP demonstrates that nearly 90% of the enriched H3K9/K14ac peaks are overlapped between biological replicates, indicating its remarkable consistency and reproducibility. CONCLUSIONS: An N-ChIP method suitable for the fleshy fruit tissues of woodland strawberry Fragaria vesca is described in this study. The efficiency and reproducibility of our optimized N-ChIP protocol are validated by both qRT-PCR and high-throughput sequencing. We conclude that N-ChIP is a more suitable method for strawberry fruit tissues relative to X-ChIP, which could be combined with high-throughput sequencing to investigate the impact of histone modifications in strawberry and potentially in other fruits with high content of polysaccharides.
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spelling pubmed-69982512020-02-05 A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits Huang, Xiaorong Pan, Qinwei Lin, Ying Gu, Tingting Li, Yi Plant Methods Methodology BACKGROUND: Covalent modifications of histones and histone variants have great influence on chromatin structure, which is involved in the transcriptional regulation of gene expression. Chromatin immunoprecipitation (ChIP) is a powerful tool for studying in vivo DNA-histone interactions. Strawberry is a model for Rosaceae and non-climacteric fruits, in which histone modifications have been implicated to affect fruit development and ripening. However, a validated ChIP method has not been reported in strawberry, probably due to its high levels of polysaccharides which affect the quality of prepared chromatin and the efficiency of immunoprecipitation. RESULTS: We describe a native chromatin immunoprecipitation (N-ChIP) protocol suitable for strawberry by optimizing the parameters for nuclei isolation, chromatin extraction, DNA fragmentation and validation analysis using quantitative real-time PCR (qRT-PCR). The qRT-PCR results show that both the active mark H3K36me3 and the silent mark H3K9me2 are efficiently immunoprecipitated for the enriched regions. Compared to X-ChIP (cross-linked chromatin followed by immunoprecipitation), our optimized N-ChIP procedure has a higher signal-to-noise ratio and a lower background for both the active and the silent histone modifications. Furthermore, high-throughput sequencing following N-ChIP demonstrates that nearly 90% of the enriched H3K9/K14ac peaks are overlapped between biological replicates, indicating its remarkable consistency and reproducibility. CONCLUSIONS: An N-ChIP method suitable for the fleshy fruit tissues of woodland strawberry Fragaria vesca is described in this study. The efficiency and reproducibility of our optimized N-ChIP protocol are validated by both qRT-PCR and high-throughput sequencing. We conclude that N-ChIP is a more suitable method for strawberry fruit tissues relative to X-ChIP, which could be combined with high-throughput sequencing to investigate the impact of histone modifications in strawberry and potentially in other fruits with high content of polysaccharides. BioMed Central 2020-02-03 /pmc/articles/PMC6998251/ /pubmed/32025237 http://dx.doi.org/10.1186/s13007-020-0556-z 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 Methodology
Huang, Xiaorong
Pan, Qinwei
Lin, Ying
Gu, Tingting
Li, Yi
A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits
title A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits
title_full A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits
title_fullStr A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits
title_full_unstemmed A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits
title_short A native chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in strawberry fruits
title_sort native chromatin immunoprecipitation (chip) protocol for studying histone modifications in strawberry fruits
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998251/
https://www.ncbi.nlm.nih.gov/pubmed/32025237
http://dx.doi.org/10.1186/s13007-020-0556-z
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