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Sirt6 is required for spermatogenesis in mice

SIRT6, a nuclear protein, has been implicated in a number of essential cellular processes, such as the DNA damage response, metabolic homeostasis, inflammation, tumorigenesis and aging. However, the role of Sirt6 in the regulation of spermatogenesis is yet unknown. In the present study, we successfu...

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Autores principales: Wei, Huafang, Khawar, Muhammad Babar, Tang, Wenhao, Wang, Lina, Wang, Liying, Liu, Chao, Jiang, Hui, Li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521524/
https://www.ncbi.nlm.nih.gov/pubmed/32915773
http://dx.doi.org/10.18632/aging.103641
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author Wei, Huafang
Khawar, Muhammad Babar
Tang, Wenhao
Wang, Lina
Wang, Liying
Liu, Chao
Jiang, Hui
Li, Wei
author_facet Wei, Huafang
Khawar, Muhammad Babar
Tang, Wenhao
Wang, Lina
Wang, Liying
Liu, Chao
Jiang, Hui
Li, Wei
author_sort Wei, Huafang
collection PubMed
description SIRT6, a nuclear protein, has been implicated in a number of essential cellular processes, such as the DNA damage response, metabolic homeostasis, inflammation, tumorigenesis and aging. However, the role of Sirt6 in the regulation of spermatogenesis is yet unknown. In the present study, we successfully generated Sirt6(-/-) mice on a C57BL6/ICR mixed background and found that some Sirt6(-/-) mice survived beyond eight weeks. We further revealed that spermatogenesis in Sirt6(-/-) mice was arrested at the elongated spermatid stage. Sirt6(-/-) male mice were completely infertile and had an increased number of apoptotic spermatids. To our surprise, deacetylation activities of SIRT6 on H3K9ac, H3K18ac and H3K56c were not required for spermatogenesis. Therefore, our findings establish a novel link between Sirt6 and male fertility, suggesting an essential role of Sirt6 in spermatogenesis.
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spelling pubmed-75215242020-10-02 Sirt6 is required for spermatogenesis in mice Wei, Huafang Khawar, Muhammad Babar Tang, Wenhao Wang, Lina Wang, Liying Liu, Chao Jiang, Hui Li, Wei Aging (Albany NY) Research Paper SIRT6, a nuclear protein, has been implicated in a number of essential cellular processes, such as the DNA damage response, metabolic homeostasis, inflammation, tumorigenesis and aging. However, the role of Sirt6 in the regulation of spermatogenesis is yet unknown. In the present study, we successfully generated Sirt6(-/-) mice on a C57BL6/ICR mixed background and found that some Sirt6(-/-) mice survived beyond eight weeks. We further revealed that spermatogenesis in Sirt6(-/-) mice was arrested at the elongated spermatid stage. Sirt6(-/-) male mice were completely infertile and had an increased number of apoptotic spermatids. To our surprise, deacetylation activities of SIRT6 on H3K9ac, H3K18ac and H3K56c were not required for spermatogenesis. Therefore, our findings establish a novel link between Sirt6 and male fertility, suggesting an essential role of Sirt6 in spermatogenesis. Impact Journals 2020-09-11 /pmc/articles/PMC7521524/ /pubmed/32915773 http://dx.doi.org/10.18632/aging.103641 Text en Copyright: © 2020 Wei et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wei, Huafang
Khawar, Muhammad Babar
Tang, Wenhao
Wang, Lina
Wang, Liying
Liu, Chao
Jiang, Hui
Li, Wei
Sirt6 is required for spermatogenesis in mice
title Sirt6 is required for spermatogenesis in mice
title_full Sirt6 is required for spermatogenesis in mice
title_fullStr Sirt6 is required for spermatogenesis in mice
title_full_unstemmed Sirt6 is required for spermatogenesis in mice
title_short Sirt6 is required for spermatogenesis in mice
title_sort sirt6 is required for spermatogenesis in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521524/
https://www.ncbi.nlm.nih.gov/pubmed/32915773
http://dx.doi.org/10.18632/aging.103641
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