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Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging
Cattle are an attractive animal model of fertility in women due to their high degree of similarity relative to follicle selection, embryo cleavage, blastocyst formation, and gestation length. To facilitate future studies of the epigenetic underpinnings of aging effects in the female reproductive axi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8135012/ https://www.ncbi.nlm.nih.gov/pubmed/33797841 http://dx.doi.org/10.1111/acel.13349 |
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author | Kordowitzki, Paweł Haghani, Amin Zoller, Joseph A. Li, Caesar Z. Raj, Ken Spangler, Matthew L. Horvath, Steve |
author_facet | Kordowitzki, Paweł Haghani, Amin Zoller, Joseph A. Li, Caesar Z. Raj, Ken Spangler, Matthew L. Horvath, Steve |
author_sort | Kordowitzki, Paweł |
collection | PubMed |
description | Cattle are an attractive animal model of fertility in women due to their high degree of similarity relative to follicle selection, embryo cleavage, blastocyst formation, and gestation length. To facilitate future studies of the epigenetic underpinnings of aging effects in the female reproductive axis, several DNA methylation‐based biomarkers of aging (epigenetic clocks) for bovine oocytes are presented. One such clock was germane to only oocytes, while a dual‐tissue clock was highly predictive of age in both oocytes and blood. Dual species clocks that apply to both humans and cattle were also developed and evaluated. These epigenetic clocks can be used to accurately estimate the biological age of oocytes. Both epigenetic clock studies and epigenome‐wide association studies revealed that blood and oocytes differ substantially with respect to aging and the underlying epigenetic signatures that potentially influence the aging process. The rate of epigenetic aging was found to be slower in oocytes compared to blood; however, oocytes appeared to begin at an older epigenetic age. The epigenetic clocks for oocytes are expected to address questions in the field of reproductive aging, including the central question: how to slow aging of oocytes. |
format | Online Article Text |
id | pubmed-8135012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81350122021-05-21 Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging Kordowitzki, Paweł Haghani, Amin Zoller, Joseph A. Li, Caesar Z. Raj, Ken Spangler, Matthew L. Horvath, Steve Aging Cell Original Articles Cattle are an attractive animal model of fertility in women due to their high degree of similarity relative to follicle selection, embryo cleavage, blastocyst formation, and gestation length. To facilitate future studies of the epigenetic underpinnings of aging effects in the female reproductive axis, several DNA methylation‐based biomarkers of aging (epigenetic clocks) for bovine oocytes are presented. One such clock was germane to only oocytes, while a dual‐tissue clock was highly predictive of age in both oocytes and blood. Dual species clocks that apply to both humans and cattle were also developed and evaluated. These epigenetic clocks can be used to accurately estimate the biological age of oocytes. Both epigenetic clock studies and epigenome‐wide association studies revealed that blood and oocytes differ substantially with respect to aging and the underlying epigenetic signatures that potentially influence the aging process. The rate of epigenetic aging was found to be slower in oocytes compared to blood; however, oocytes appeared to begin at an older epigenetic age. The epigenetic clocks for oocytes are expected to address questions in the field of reproductive aging, including the central question: how to slow aging of oocytes. John Wiley and Sons Inc. 2021-04-02 2021-05 /pmc/articles/PMC8135012/ /pubmed/33797841 http://dx.doi.org/10.1111/acel.13349 Text en © 2021 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kordowitzki, Paweł Haghani, Amin Zoller, Joseph A. Li, Caesar Z. Raj, Ken Spangler, Matthew L. Horvath, Steve Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
title | Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
title_full | Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
title_fullStr | Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
title_full_unstemmed | Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
title_short | Epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
title_sort | epigenetic clock and methylation study of oocytes from a bovine model of reproductive aging |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8135012/ https://www.ncbi.nlm.nih.gov/pubmed/33797841 http://dx.doi.org/10.1111/acel.13349 |
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