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DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation
BACKGROUND: The association of in vitro fertilisation (IVF) and DNA methylation has been studied predominantly at regulatory regions of imprinted genes and at just thousands of the ~28 million CpG sites in the human genome. METHODS: We investigated the links between IVF and DNA methylation patterns...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364659/ https://www.ncbi.nlm.nih.gov/pubmed/28340599 http://dx.doi.org/10.1186/s13073-017-0413-5 |
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author | Castillo-Fernandez, Juan E. Loke, Yuk Jing Bass-Stringer, Sebastian Gao, Fei Xia, Yudong Wu, Honglong Lu, Hanlin Liu, Yuan Wang, Jun Spector, Tim D. Saffery, Richard Craig, Jeffrey M. Bell, Jordana T. |
author_facet | Castillo-Fernandez, Juan E. Loke, Yuk Jing Bass-Stringer, Sebastian Gao, Fei Xia, Yudong Wu, Honglong Lu, Hanlin Liu, Yuan Wang, Jun Spector, Tim D. Saffery, Richard Craig, Jeffrey M. Bell, Jordana T. |
author_sort | Castillo-Fernandez, Juan E. |
collection | PubMed |
description | BACKGROUND: The association of in vitro fertilisation (IVF) and DNA methylation has been studied predominantly at regulatory regions of imprinted genes and at just thousands of the ~28 million CpG sites in the human genome. METHODS: We investigated the links between IVF and DNA methylation patterns in whole cord blood cells (n = 98) and cord blood mononuclear cells (n = 82) from newborn twins using genome-wide methylated DNA immunoprecipitation coupled with deep sequencing. RESULTS: At a false discovery rate (FDR) of 5%, we identified one significant whole blood DNA methylation change linked to conception via IVF, which was located ~3 kb upstream of TNP1, a gene previously linked to male infertility. The 46 most strongly associated signals (FDR of 25%) included a second region in a gene also previously linked to infertility, C9orf3, suggesting that our findings may in part capture the effect of parental subfertility. Using twin modelling, we observed that individual-specific environmental factors appear to be the main overall contributors of methylation variability at the FDR 25% IVF-associated differentially methylated regions, although evidence for methylation heritability was also obtained at several of these regions. We replicated previous findings of differential methylation associated with IVF at the H19/IGF2 region in cord blood mononuclear cells, and we validated the signal at C9orf3 in monozygotic twins. We also explored the impact of intracytoplasmic sperm injection on the FDR 25% signals for potential effects specific to male or female infertility factors. CONCLUSIONS: To our knowledge, this is the most comprehensive study of DNA methylation profiles at birth and IVF conception to date, and our results show evidence for epigenetic modifications that may in part reflect parental subfertility. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-017-0413-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5364659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53646592017-03-24 DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation Castillo-Fernandez, Juan E. Loke, Yuk Jing Bass-Stringer, Sebastian Gao, Fei Xia, Yudong Wu, Honglong Lu, Hanlin Liu, Yuan Wang, Jun Spector, Tim D. Saffery, Richard Craig, Jeffrey M. Bell, Jordana T. Genome Med Research BACKGROUND: The association of in vitro fertilisation (IVF) and DNA methylation has been studied predominantly at regulatory regions of imprinted genes and at just thousands of the ~28 million CpG sites in the human genome. METHODS: We investigated the links between IVF and DNA methylation patterns in whole cord blood cells (n = 98) and cord blood mononuclear cells (n = 82) from newborn twins using genome-wide methylated DNA immunoprecipitation coupled with deep sequencing. RESULTS: At a false discovery rate (FDR) of 5%, we identified one significant whole blood DNA methylation change linked to conception via IVF, which was located ~3 kb upstream of TNP1, a gene previously linked to male infertility. The 46 most strongly associated signals (FDR of 25%) included a second region in a gene also previously linked to infertility, C9orf3, suggesting that our findings may in part capture the effect of parental subfertility. Using twin modelling, we observed that individual-specific environmental factors appear to be the main overall contributors of methylation variability at the FDR 25% IVF-associated differentially methylated regions, although evidence for methylation heritability was also obtained at several of these regions. We replicated previous findings of differential methylation associated with IVF at the H19/IGF2 region in cord blood mononuclear cells, and we validated the signal at C9orf3 in monozygotic twins. We also explored the impact of intracytoplasmic sperm injection on the FDR 25% signals for potential effects specific to male or female infertility factors. CONCLUSIONS: To our knowledge, this is the most comprehensive study of DNA methylation profiles at birth and IVF conception to date, and our results show evidence for epigenetic modifications that may in part reflect parental subfertility. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-017-0413-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-24 /pmc/articles/PMC5364659/ /pubmed/28340599 http://dx.doi.org/10.1186/s13073-017-0413-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Castillo-Fernandez, Juan E. Loke, Yuk Jing Bass-Stringer, Sebastian Gao, Fei Xia, Yudong Wu, Honglong Lu, Hanlin Liu, Yuan Wang, Jun Spector, Tim D. Saffery, Richard Craig, Jeffrey M. Bell, Jordana T. DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
title | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
title_full | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
title_fullStr | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
title_full_unstemmed | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
title_short | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
title_sort | dna methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364659/ https://www.ncbi.nlm.nih.gov/pubmed/28340599 http://dx.doi.org/10.1186/s13073-017-0413-5 |
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