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Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance
BACKGROUND: The potential that adolescent chemotherapy can impact the epigenetic programming of the germ line to influence later life adult fertility and promote epigenetic inheritance was investigated. Previous studies have demonstrated a number of environmental exposures such as abnormal nutrition...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287489/ https://www.ncbi.nlm.nih.gov/pubmed/28146567 http://dx.doi.org/10.1371/journal.pone.0170085 |
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author | Shnorhavorian, Margarett Schwartz, Stephen M. Stansfeld, Barbara Sadler-Riggleman, Ingrid Beck, Daniel Skinner, Michael K. |
author_facet | Shnorhavorian, Margarett Schwartz, Stephen M. Stansfeld, Barbara Sadler-Riggleman, Ingrid Beck, Daniel Skinner, Michael K. |
author_sort | Shnorhavorian, Margarett |
collection | PubMed |
description | BACKGROUND: The potential that adolescent chemotherapy can impact the epigenetic programming of the germ line to influence later life adult fertility and promote epigenetic inheritance was investigated. Previous studies have demonstrated a number of environmental exposures such as abnormal nutrition and toxicants can promote sperm epigenetic changes that impact offspring. METHODS: Adult males approximately ten years after pubertal exposure to chemotherapy were compared to adult males with no previous exposure. Sperm were collected to examine differential DNA methylation regions (DMRs) between the exposed and control populations. Gene associations and correlations to genetic mutations (copy number variation) were also investigated. METHODS AND FINDINGS: A signature of statistically significant DMRs was identified in the chemotherapy exposed male sperm. The DMRs, termed epimutations, were found in CpG desert regions of primarily 1 kilobase size. Observations indicate adolescent chemotherapy exposure can promote epigenetic alterations that persist in later life. CONCLUSIONS: This is the first observation in humans that an early life chemical exposure can permanently reprogram the spermatogenic stem cell epigenome. The germline (i.e., sperm) epimutations identified suggest chemotherapy has the potential to promote epigenetic inheritance to the next generation. |
format | Online Article Text |
id | pubmed-5287489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52874892017-02-17 Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance Shnorhavorian, Margarett Schwartz, Stephen M. Stansfeld, Barbara Sadler-Riggleman, Ingrid Beck, Daniel Skinner, Michael K. PLoS One Research Article BACKGROUND: The potential that adolescent chemotherapy can impact the epigenetic programming of the germ line to influence later life adult fertility and promote epigenetic inheritance was investigated. Previous studies have demonstrated a number of environmental exposures such as abnormal nutrition and toxicants can promote sperm epigenetic changes that impact offspring. METHODS: Adult males approximately ten years after pubertal exposure to chemotherapy were compared to adult males with no previous exposure. Sperm were collected to examine differential DNA methylation regions (DMRs) between the exposed and control populations. Gene associations and correlations to genetic mutations (copy number variation) were also investigated. METHODS AND FINDINGS: A signature of statistically significant DMRs was identified in the chemotherapy exposed male sperm. The DMRs, termed epimutations, were found in CpG desert regions of primarily 1 kilobase size. Observations indicate adolescent chemotherapy exposure can promote epigenetic alterations that persist in later life. CONCLUSIONS: This is the first observation in humans that an early life chemical exposure can permanently reprogram the spermatogenic stem cell epigenome. The germline (i.e., sperm) epimutations identified suggest chemotherapy has the potential to promote epigenetic inheritance to the next generation. Public Library of Science 2017-02-01 /pmc/articles/PMC5287489/ /pubmed/28146567 http://dx.doi.org/10.1371/journal.pone.0170085 Text en © 2017 Shnorhavorian et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Shnorhavorian, Margarett Schwartz, Stephen M. Stansfeld, Barbara Sadler-Riggleman, Ingrid Beck, Daniel Skinner, Michael K. Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance |
title | Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance |
title_full | Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance |
title_fullStr | Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance |
title_full_unstemmed | Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance |
title_short | Differential DNA Methylation Regions in Adult Human Sperm following Adolescent Chemotherapy: Potential for Epigenetic Inheritance |
title_sort | differential dna methylation regions in adult human sperm following adolescent chemotherapy: potential for epigenetic inheritance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287489/ https://www.ncbi.nlm.nih.gov/pubmed/28146567 http://dx.doi.org/10.1371/journal.pone.0170085 |
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