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SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development

BACKGROUND: The histone code is an established epigenetic regulator of early embryonic development in mammals. The lysine residue K9 of histone H3 (H3K9) is a prime target of SIRT1, a member of NAD(+)-dependent histone deacetylase family of enzymes targeting both histone and non-histone substrates....

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Autores principales: Adamkova, Katerina, Yi, Young-Joo, Petr, Jaroslav, Zalmanova, Tereza, Hoskova, Kristyna, Jelinkova, Pavla, Moravec, Jiri, Kralickova, Milena, Sutovsky, Miriam, Sutovsky, Peter, Nevoral, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664433/
https://www.ncbi.nlm.nih.gov/pubmed/29118980
http://dx.doi.org/10.1186/s40104-017-0214-0
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author Adamkova, Katerina
Yi, Young-Joo
Petr, Jaroslav
Zalmanova, Tereza
Hoskova, Kristyna
Jelinkova, Pavla
Moravec, Jiri
Kralickova, Milena
Sutovsky, Miriam
Sutovsky, Peter
Nevoral, Jan
author_facet Adamkova, Katerina
Yi, Young-Joo
Petr, Jaroslav
Zalmanova, Tereza
Hoskova, Kristyna
Jelinkova, Pavla
Moravec, Jiri
Kralickova, Milena
Sutovsky, Miriam
Sutovsky, Peter
Nevoral, Jan
author_sort Adamkova, Katerina
collection PubMed
description BACKGROUND: The histone code is an established epigenetic regulator of early embryonic development in mammals. The lysine residue K9 of histone H3 (H3K9) is a prime target of SIRT1, a member of NAD(+)-dependent histone deacetylase family of enzymes targeting both histone and non-histone substrates. At present, little is known about SIRT1-modulation of H3K9 in zygotic pronuclei and its association with the success of preimplantation embryo development. Therefore, we evaluated the effect of SIRT1 activity on H3K9 methylation and acetylation in porcine zygotes and the significance of H3K9 modifications for early embryonic development. RESULTS: Our results show that SIRT1 activators resveratrol and BML-278 increased H3K9 methylation and suppressed H3K9 acetylation in both the paternal and maternal pronucleus. Inversely, SIRT1 inhibitors nicotinamide and sirtinol suppressed methylation and increased acetylation of pronuclear H3K9. Evaluation of early embryonic development confirmed positive effect of selective SIRT1 activation on blastocyst formation rate (5.2 ± 2.9% versus 32.9 ± 8.1% in vehicle control and BML-278 group, respectively; P ≤ 0.05). Stimulation of SIRT1 activity coincided with fluorometric signal intensity of ooplasmic ubiquitin ligase MDM2, a known substrate of SIRT1 and known limiting factor of epigenome remodeling. CONCLUSIONS: We conclude that SIRT1 modulates zygotic histone code, obviously through direct deacetylation and via non-histone targets resulting in increased H3K9me3. These changes in zygotes lead to more successful pre-implantation embryonic development and, indeed, the specific SIRT1 activation due to BML-278 is beneficial for in vitro embryo production and blastocyst achievement. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-017-0214-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-56644332017-11-08 SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development Adamkova, Katerina Yi, Young-Joo Petr, Jaroslav Zalmanova, Tereza Hoskova, Kristyna Jelinkova, Pavla Moravec, Jiri Kralickova, Milena Sutovsky, Miriam Sutovsky, Peter Nevoral, Jan J Anim Sci Biotechnol Research BACKGROUND: The histone code is an established epigenetic regulator of early embryonic development in mammals. The lysine residue K9 of histone H3 (H3K9) is a prime target of SIRT1, a member of NAD(+)-dependent histone deacetylase family of enzymes targeting both histone and non-histone substrates. At present, little is known about SIRT1-modulation of H3K9 in zygotic pronuclei and its association with the success of preimplantation embryo development. Therefore, we evaluated the effect of SIRT1 activity on H3K9 methylation and acetylation in porcine zygotes and the significance of H3K9 modifications for early embryonic development. RESULTS: Our results show that SIRT1 activators resveratrol and BML-278 increased H3K9 methylation and suppressed H3K9 acetylation in both the paternal and maternal pronucleus. Inversely, SIRT1 inhibitors nicotinamide and sirtinol suppressed methylation and increased acetylation of pronuclear H3K9. Evaluation of early embryonic development confirmed positive effect of selective SIRT1 activation on blastocyst formation rate (5.2 ± 2.9% versus 32.9 ± 8.1% in vehicle control and BML-278 group, respectively; P ≤ 0.05). Stimulation of SIRT1 activity coincided with fluorometric signal intensity of ooplasmic ubiquitin ligase MDM2, a known substrate of SIRT1 and known limiting factor of epigenome remodeling. CONCLUSIONS: We conclude that SIRT1 modulates zygotic histone code, obviously through direct deacetylation and via non-histone targets resulting in increased H3K9me3. These changes in zygotes lead to more successful pre-implantation embryonic development and, indeed, the specific SIRT1 activation due to BML-278 is beneficial for in vitro embryo production and blastocyst achievement. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-017-0214-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-01 /pmc/articles/PMC5664433/ /pubmed/29118980 http://dx.doi.org/10.1186/s40104-017-0214-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.
spellingShingle Research
Adamkova, Katerina
Yi, Young-Joo
Petr, Jaroslav
Zalmanova, Tereza
Hoskova, Kristyna
Jelinkova, Pavla
Moravec, Jiri
Kralickova, Milena
Sutovsky, Miriam
Sutovsky, Peter
Nevoral, Jan
SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development
title SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development
title_full SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development
title_fullStr SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development
title_full_unstemmed SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development
title_short SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development
title_sort sirt1-dependent modulation of methylation and acetylation of histone h3 on lysine 9 (h3k9) in the zygotic pronuclei improves porcine embryo development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664433/
https://www.ncbi.nlm.nih.gov/pubmed/29118980
http://dx.doi.org/10.1186/s40104-017-0214-0
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