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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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