Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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
_version_ 1782517368244666368
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
work_keys_str_mv AT castillofernandezjuane dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT lokeyukjing dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT bassstringersebastian dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT gaofei dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT xiayudong dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT wuhonglong dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT luhanlin dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT liuyuan dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT wangjun dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT spectortimd dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT safferyrichard dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT craigjeffreym dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation
AT belljordanat dnamethylationchangesatinfertilitygenesinnewborntwinsconceivedbyinvitrofertilisation