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Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)

Genomic imprinting occurs before fertilization, impacts every cell of the developing child, and may be sensitive to environmental perturbations. The noncoding RNA, nc886 (also called VTRNA2-1) is the only known example of the ∼100 human genes imprinted by DNA methylation, that shows polymorphic impr...

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Autores principales: Carpenter, Brittany L., Remba, Tanaka K., Thomas, Stacey L., Madaj, Zachary, Brink, Lucy, Tiedemann, Rochelle L., Odendaal, Hein J., Jones, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000112/
https://www.ncbi.nlm.nih.gov/pubmed/33723081
http://dx.doi.org/10.1073/pnas.2026580118
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author Carpenter, Brittany L.
Remba, Tanaka K.
Thomas, Stacey L.
Madaj, Zachary
Brink, Lucy
Tiedemann, Rochelle L.
Odendaal, Hein J.
Jones, Peter A.
author_facet Carpenter, Brittany L.
Remba, Tanaka K.
Thomas, Stacey L.
Madaj, Zachary
Brink, Lucy
Tiedemann, Rochelle L.
Odendaal, Hein J.
Jones, Peter A.
author_sort Carpenter, Brittany L.
collection PubMed
description Genomic imprinting occurs before fertilization, impacts every cell of the developing child, and may be sensitive to environmental perturbations. The noncoding RNA, nc886 (also called VTRNA2-1) is the only known example of the ∼100 human genes imprinted by DNA methylation, that shows polymorphic imprinting in the population. The nc886 gene is part of an ∼1.6-kb differentially methylated region (DMR) that is methylated in the oocyte and silenced on the maternal allele in about 75% of humans worldwide. Here, we show that the presence or absence of imprinting at the nc886 DMR in an individual is consistent across different tissues, confirming that the imprint is established before cellular differentiation and is maintained into adulthood. We investigated the relationships between the frequency of imprinting in newborns and maternal age, alcohol consumption and cigarette smoking before conception in more than 1,100 mother/child pairs from South Africa. The probability of imprinting in newborns was increased in older mothers and decreased in mothers who drank alcohol before conception. On the other hand, cigarette smoking had no apparent relationship with the frequency of imprinting. These data show an epigenetic change during oocyte maturation which is potentially subject to environmental influence. Much focus has been placed on avoiding alcohol consumption during pregnancy, but our data suggest that drinking before conception may affect the epigenome of the newborn.
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spelling pubmed-80001122021-04-01 Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886) Carpenter, Brittany L. Remba, Tanaka K. Thomas, Stacey L. Madaj, Zachary Brink, Lucy Tiedemann, Rochelle L. Odendaal, Hein J. Jones, Peter A. Proc Natl Acad Sci U S A Biological Sciences Genomic imprinting occurs before fertilization, impacts every cell of the developing child, and may be sensitive to environmental perturbations. The noncoding RNA, nc886 (also called VTRNA2-1) is the only known example of the ∼100 human genes imprinted by DNA methylation, that shows polymorphic imprinting in the population. The nc886 gene is part of an ∼1.6-kb differentially methylated region (DMR) that is methylated in the oocyte and silenced on the maternal allele in about 75% of humans worldwide. Here, we show that the presence or absence of imprinting at the nc886 DMR in an individual is consistent across different tissues, confirming that the imprint is established before cellular differentiation and is maintained into adulthood. We investigated the relationships between the frequency of imprinting in newborns and maternal age, alcohol consumption and cigarette smoking before conception in more than 1,100 mother/child pairs from South Africa. The probability of imprinting in newborns was increased in older mothers and decreased in mothers who drank alcohol before conception. On the other hand, cigarette smoking had no apparent relationship with the frequency of imprinting. These data show an epigenetic change during oocyte maturation which is potentially subject to environmental influence. Much focus has been placed on avoiding alcohol consumption during pregnancy, but our data suggest that drinking before conception may affect the epigenome of the newborn. National Academy of Sciences 2021-03-23 2021-03-15 /pmc/articles/PMC8000112/ /pubmed/33723081 http://dx.doi.org/10.1073/pnas.2026580118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Carpenter, Brittany L.
Remba, Tanaka K.
Thomas, Stacey L.
Madaj, Zachary
Brink, Lucy
Tiedemann, Rochelle L.
Odendaal, Hein J.
Jones, Peter A.
Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)
title Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)
title_full Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)
title_fullStr Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)
title_full_unstemmed Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)
title_short Oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding RNA (nc886)
title_sort oocyte age and preconceptual alcohol use are highly correlated with epigenetic imprinting of a noncoding rna (nc886)
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000112/
https://www.ncbi.nlm.nih.gov/pubmed/33723081
http://dx.doi.org/10.1073/pnas.2026580118
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