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Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo
The health of the offspring depends on the genetic constitution of the parental germ cells. The paternal genome appears to be important; e.g., de novo mutations in some genes seem to arise mostly from the father, whereas epigenetic modifications of DNA and histones are frequent in the paternal gonad...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430208/ https://www.ncbi.nlm.nih.gov/pubmed/22641617 http://dx.doi.org/10.1093/toxsci/kfs187 |
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author | Brevik, Asgeir Lindeman, Birgitte Rusnakova, Vendula Olsen, Ann-Karin Brunborg, Gunnar Duale, Nur |
author_facet | Brevik, Asgeir Lindeman, Birgitte Rusnakova, Vendula Olsen, Ann-Karin Brunborg, Gunnar Duale, Nur |
author_sort | Brevik, Asgeir |
collection | PubMed |
description | The health of the offspring depends on the genetic constitution of the parental germ cells. The paternal genome appears to be important; e.g., de novo mutations in some genes seem to arise mostly from the father, whereas epigenetic modifications of DNA and histones are frequent in the paternal gonads. Environmental contaminants which may affect the integrity of the germ cells comprise the polycyclic aromatic hydrocarbon, benzo[a]pyrene (B[a]P). B[a]P has received much attention due to its ubiquitous distribution, its carcinogenic and mutagenic potential, and also effects on reproduction. We conducted an in vitro fertilization (IVF) experiment using sperm cells from B[a]P-exposed male mice to study effects of paternal B[a]P exposure on early gene expression in the developing mouse embryo. Male mice were exposed to a single acute dose of B[a]P (150mg/kg, ip) 4 days prior to isolation of cauda sperm, followed by IVF of oocytes from unexposed superovulated mice. Gene expression in fertilized zygotes/embryos was determined using reverse transcription-qPCR at the 1-, 2-, 4-, 8-, and blastocyst cell stages of embryo development. We found that paternal B[a]P exposure altered the expression of numerous genes in the developing embryo especially at the blastocyst stage. Some genes were also affected at earlier developmental stages. Embryonic gene expression studies seem useful to identify perturbations of signaling pathways resulting from exposure to contaminants, and can be used to address mechanisms of paternal effects on embryo development. |
format | Online Article Text |
id | pubmed-3430208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34302082012-08-29 Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo Brevik, Asgeir Lindeman, Birgitte Rusnakova, Vendula Olsen, Ann-Karin Brunborg, Gunnar Duale, Nur Toxicol Sci Research Article The health of the offspring depends on the genetic constitution of the parental germ cells. The paternal genome appears to be important; e.g., de novo mutations in some genes seem to arise mostly from the father, whereas epigenetic modifications of DNA and histones are frequent in the paternal gonads. Environmental contaminants which may affect the integrity of the germ cells comprise the polycyclic aromatic hydrocarbon, benzo[a]pyrene (B[a]P). B[a]P has received much attention due to its ubiquitous distribution, its carcinogenic and mutagenic potential, and also effects on reproduction. We conducted an in vitro fertilization (IVF) experiment using sperm cells from B[a]P-exposed male mice to study effects of paternal B[a]P exposure on early gene expression in the developing mouse embryo. Male mice were exposed to a single acute dose of B[a]P (150mg/kg, ip) 4 days prior to isolation of cauda sperm, followed by IVF of oocytes from unexposed superovulated mice. Gene expression in fertilized zygotes/embryos was determined using reverse transcription-qPCR at the 1-, 2-, 4-, 8-, and blastocyst cell stages of embryo development. We found that paternal B[a]P exposure altered the expression of numerous genes in the developing embryo especially at the blastocyst stage. Some genes were also affected at earlier developmental stages. Embryonic gene expression studies seem useful to identify perturbations of signaling pathways resulting from exposure to contaminants, and can be used to address mechanisms of paternal effects on embryo development. Oxford University Press 2012-09 2012-05-28 /pmc/articles/PMC3430208/ /pubmed/22641617 http://dx.doi.org/10.1093/toxsci/kfs187 Text en © The Author 2012. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: journals.permissions@oup.com This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0/uk/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Brevik, Asgeir Lindeman, Birgitte Rusnakova, Vendula Olsen, Ann-Karin Brunborg, Gunnar Duale, Nur Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo |
title | Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo |
title_full | Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo |
title_fullStr | Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo |
title_full_unstemmed | Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo |
title_short | Paternal Benzo[a]pyrene Exposure Affects Gene Expression in the Early Developing Mouse Embryo |
title_sort | paternal benzo[a]pyrene exposure affects gene expression in the early developing mouse embryo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430208/ https://www.ncbi.nlm.nih.gov/pubmed/22641617 http://dx.doi.org/10.1093/toxsci/kfs187 |
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