Cargando…
Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato
Fruit formation comprises a series of developmental transitions among which the fruit set process is essential in determining crop yield. Yet, our understanding of the epigenetic landscape remodelling associated with the flower‐to‐fruit transition remains poor. We investigated the epigenetic and tra...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821339/ https://www.ncbi.nlm.nih.gov/pubmed/32875585 http://dx.doi.org/10.1111/nph.16902 |
_version_ | 1783639402879123456 |
---|---|
author | Hu, Guojian Huang, Baowen Wang, Keke Frasse, Pierre Maza, Elie Djari, Anis Benhamed, Moussa Gallusci, Philippe Li, Zhengguo Zouine, Mohamed Bouzayen, Mondher |
author_facet | Hu, Guojian Huang, Baowen Wang, Keke Frasse, Pierre Maza, Elie Djari, Anis Benhamed, Moussa Gallusci, Philippe Li, Zhengguo Zouine, Mohamed Bouzayen, Mondher |
author_sort | Hu, Guojian |
collection | PubMed |
description | Fruit formation comprises a series of developmental transitions among which the fruit set process is essential in determining crop yield. Yet, our understanding of the epigenetic landscape remodelling associated with the flower‐to‐fruit transition remains poor. We investigated the epigenetic and transcriptomic reprogramming underlying pollination‐dependent and auxin‐induced flower‐to‐fruit transitions in the tomato (Solanum lycopersicum) using combined genomewide transcriptomic profiling, global ChIP‐sequencing and whole genomic DNA bisulfite sequencing (WGBS). Variation in the expression of the overwhelming majority of genes was associated with change in histone mark distribution, whereas changes in DNA methylation concerned a minor fraction of differentially expressed genes. Reprogramming of genes involved in processes instrumental to fruit set correlated with their H3K9ac or H3K4me3 marking status but not with changes in cytosine methylation, indicating that histone posttranslational modifications rather than DNA methylation are associated with the remodelling of the epigenetic landscape underpinning the flower‐to‐fruit transition. Given the prominent role previously assigned to DNA methylation in reprogramming key genes of the transition to ripening, the outcome of the present study supports the idea that the two main developmental transitions in fleshy fruit and the underlying transcriptomic reprogramming are associated with different modes of epigenetic regulations. |
format | Online Article Text |
id | pubmed-7821339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78213392021-02-01 Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato Hu, Guojian Huang, Baowen Wang, Keke Frasse, Pierre Maza, Elie Djari, Anis Benhamed, Moussa Gallusci, Philippe Li, Zhengguo Zouine, Mohamed Bouzayen, Mondher New Phytol Research Fruit formation comprises a series of developmental transitions among which the fruit set process is essential in determining crop yield. Yet, our understanding of the epigenetic landscape remodelling associated with the flower‐to‐fruit transition remains poor. We investigated the epigenetic and transcriptomic reprogramming underlying pollination‐dependent and auxin‐induced flower‐to‐fruit transitions in the tomato (Solanum lycopersicum) using combined genomewide transcriptomic profiling, global ChIP‐sequencing and whole genomic DNA bisulfite sequencing (WGBS). Variation in the expression of the overwhelming majority of genes was associated with change in histone mark distribution, whereas changes in DNA methylation concerned a minor fraction of differentially expressed genes. Reprogramming of genes involved in processes instrumental to fruit set correlated with their H3K9ac or H3K4me3 marking status but not with changes in cytosine methylation, indicating that histone posttranslational modifications rather than DNA methylation are associated with the remodelling of the epigenetic landscape underpinning the flower‐to‐fruit transition. Given the prominent role previously assigned to DNA methylation in reprogramming key genes of the transition to ripening, the outcome of the present study supports the idea that the two main developmental transitions in fleshy fruit and the underlying transcriptomic reprogramming are associated with different modes of epigenetic regulations. John Wiley and Sons Inc. 2020-10-27 2021-01 /pmc/articles/PMC7821339/ /pubmed/32875585 http://dx.doi.org/10.1111/nph.16902 Text en ©2020 The Authors New Phytologist ©2020 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Hu, Guojian Huang, Baowen Wang, Keke Frasse, Pierre Maza, Elie Djari, Anis Benhamed, Moussa Gallusci, Philippe Li, Zhengguo Zouine, Mohamed Bouzayen, Mondher Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
title | Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
title_full | Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
title_fullStr | Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
title_full_unstemmed | Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
title_short | Histone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
title_sort | histone posttranslational modifications rather than dna methylation underlie gene reprogramming in pollination‐dependent and pollination‐independent fruit set in tomato |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821339/ https://www.ncbi.nlm.nih.gov/pubmed/32875585 http://dx.doi.org/10.1111/nph.16902 |
work_keys_str_mv | AT huguojian histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT huangbaowen histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT wangkeke histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT frassepierre histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT mazaelie histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT djarianis histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT benhamedmoussa histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT gallusciphilippe histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT lizhengguo histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT zouinemohamed histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato AT bouzayenmondher histoneposttranslationalmodificationsratherthandnamethylationunderliegenereprogramminginpollinationdependentandpollinationindependentfruitsetintomato |