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Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming
Orchestrated events, including extensive changes in epigenetic marks, allow a somatic nucleus to become totipotent after transfer into an oocyte, a process termed nuclear reprogramming. Recently, several strategies have been applied in order to improve reprogramming efficiency, mainly focused on rem...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359371/ https://www.ncbi.nlm.nih.gov/pubmed/32661262 http://dx.doi.org/10.1038/s41598-020-67733-9 |
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author | Sampaio, Rafael Vilar Sangalli, Juliano Rodrigues De Bem, Tiago Henrique Camara Ambrizi, Dewison Ricardo del Collado, Maite Bridi, Alessandra de Ávila, Ana Clara Faquineli Cavalcante Mendes Macabelli, Carolina Habermann de Jesus Oliveira, Lilian da Silveira, Juliano Coelho Chiaratti, Marcos Roberto Perecin, Felipe Bressan, Fabiana Fernandes Smith, Lawrence Charles Ross, Pablo J Meirelles, Flávio Vieira |
author_facet | Sampaio, Rafael Vilar Sangalli, Juliano Rodrigues De Bem, Tiago Henrique Camara Ambrizi, Dewison Ricardo del Collado, Maite Bridi, Alessandra de Ávila, Ana Clara Faquineli Cavalcante Mendes Macabelli, Carolina Habermann de Jesus Oliveira, Lilian da Silveira, Juliano Coelho Chiaratti, Marcos Roberto Perecin, Felipe Bressan, Fabiana Fernandes Smith, Lawrence Charles Ross, Pablo J Meirelles, Flávio Vieira |
author_sort | Sampaio, Rafael Vilar |
collection | PubMed |
description | Orchestrated events, including extensive changes in epigenetic marks, allow a somatic nucleus to become totipotent after transfer into an oocyte, a process termed nuclear reprogramming. Recently, several strategies have been applied in order to improve reprogramming efficiency, mainly focused on removing repressive epigenetic marks such as histone methylation from the somatic nucleus. Herein we used the specific and non-toxic chemical probe UNC0638 to inhibit the catalytic activity of the histone methyltransferases EHMT1 and EHMT2. Either the donor cell (before reconstruction) or the early embryo was exposed to the probe to assess its effect on developmental rates and epigenetic marks. First, we showed that the treatment of bovine fibroblasts with UNC0638 did mitigate the levels of H3K9me2. Moreover, H3K9me2 levels were decreased in cloned embryos regardless of treating either donor cells or early embryos with UNC0638. Additional epigenetic marks such as H3K9me3, 5mC, and 5hmC were also affected by the UNC0638 treatment. Therefore, the use of UNC0638 did diminish the levels of H3K9me2 and H3K9me3 in SCNT-derived blastocysts, but this was unable to improve their preimplantation development. These results indicate that the specific reduction of H3K9me2 by inhibiting EHMT1/2 during nuclear reprogramming impacts the levels of H3K9me3, 5mC, and 5hmC in preimplantation bovine embryos. |
format | Online Article Text |
id | pubmed-7359371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73593712020-07-16 Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming Sampaio, Rafael Vilar Sangalli, Juliano Rodrigues De Bem, Tiago Henrique Camara Ambrizi, Dewison Ricardo del Collado, Maite Bridi, Alessandra de Ávila, Ana Clara Faquineli Cavalcante Mendes Macabelli, Carolina Habermann de Jesus Oliveira, Lilian da Silveira, Juliano Coelho Chiaratti, Marcos Roberto Perecin, Felipe Bressan, Fabiana Fernandes Smith, Lawrence Charles Ross, Pablo J Meirelles, Flávio Vieira Sci Rep Article Orchestrated events, including extensive changes in epigenetic marks, allow a somatic nucleus to become totipotent after transfer into an oocyte, a process termed nuclear reprogramming. Recently, several strategies have been applied in order to improve reprogramming efficiency, mainly focused on removing repressive epigenetic marks such as histone methylation from the somatic nucleus. Herein we used the specific and non-toxic chemical probe UNC0638 to inhibit the catalytic activity of the histone methyltransferases EHMT1 and EHMT2. Either the donor cell (before reconstruction) or the early embryo was exposed to the probe to assess its effect on developmental rates and epigenetic marks. First, we showed that the treatment of bovine fibroblasts with UNC0638 did mitigate the levels of H3K9me2. Moreover, H3K9me2 levels were decreased in cloned embryos regardless of treating either donor cells or early embryos with UNC0638. Additional epigenetic marks such as H3K9me3, 5mC, and 5hmC were also affected by the UNC0638 treatment. Therefore, the use of UNC0638 did diminish the levels of H3K9me2 and H3K9me3 in SCNT-derived blastocysts, but this was unable to improve their preimplantation development. These results indicate that the specific reduction of H3K9me2 by inhibiting EHMT1/2 during nuclear reprogramming impacts the levels of H3K9me3, 5mC, and 5hmC in preimplantation bovine embryos. Nature Publishing Group UK 2020-07-13 /pmc/articles/PMC7359371/ /pubmed/32661262 http://dx.doi.org/10.1038/s41598-020-67733-9 Text en © The Author(s) 2021, corrected publication 2021 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sampaio, Rafael Vilar Sangalli, Juliano Rodrigues De Bem, Tiago Henrique Camara Ambrizi, Dewison Ricardo del Collado, Maite Bridi, Alessandra de Ávila, Ana Clara Faquineli Cavalcante Mendes Macabelli, Carolina Habermann de Jesus Oliveira, Lilian da Silveira, Juliano Coelho Chiaratti, Marcos Roberto Perecin, Felipe Bressan, Fabiana Fernandes Smith, Lawrence Charles Ross, Pablo J Meirelles, Flávio Vieira Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
title | Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
title_full | Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
title_fullStr | Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
title_full_unstemmed | Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
title_short | Catalytic inhibition of H3K9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
title_sort | catalytic inhibition of h3k9me2 writers disturbs epigenetic marks during bovine nuclear reprogramming |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359371/ https://www.ncbi.nlm.nih.gov/pubmed/32661262 http://dx.doi.org/10.1038/s41598-020-67733-9 |
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