Cargando…

Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms

BACKGROUND: We previously showed that continued folic acid (FA) supplementation beyond the first trimester of pregnancy appears to have beneficial effects on neurocognitive performance in children followed for up to 11 years, but the biological mechanism for this effect has remained unclear. Using s...

Descripción completa

Detalles Bibliográficos
Autores principales: Ondičová, Miroslava, Irwin, Rachelle E., Thursby, Sara-Jayne, Hilman, Luke, Caffrey, Aoife, Cassidy, Tony, McLaughlin, Marian, Lees-Murdock, Diane J., Ward, Mary, Murphy, Michelle, Lamers, Yvonne, Pentieva, Kristina, McNulty, Helene, Walsh, Colum P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112484/
https://www.ncbi.nlm.nih.gov/pubmed/35578268
http://dx.doi.org/10.1186/s13148-022-01282-y
_version_ 1784709423630909440
author Ondičová, Miroslava
Irwin, Rachelle E.
Thursby, Sara-Jayne
Hilman, Luke
Caffrey, Aoife
Cassidy, Tony
McLaughlin, Marian
Lees-Murdock, Diane J.
Ward, Mary
Murphy, Michelle
Lamers, Yvonne
Pentieva, Kristina
McNulty, Helene
Walsh, Colum P.
author_facet Ondičová, Miroslava
Irwin, Rachelle E.
Thursby, Sara-Jayne
Hilman, Luke
Caffrey, Aoife
Cassidy, Tony
McLaughlin, Marian
Lees-Murdock, Diane J.
Ward, Mary
Murphy, Michelle
Lamers, Yvonne
Pentieva, Kristina
McNulty, Helene
Walsh, Colum P.
author_sort Ondičová, Miroslava
collection PubMed
description BACKGROUND: We previously showed that continued folic acid (FA) supplementation beyond the first trimester of pregnancy appears to have beneficial effects on neurocognitive performance in children followed for up to 11 years, but the biological mechanism for this effect has remained unclear. Using samples from our randomized controlled trial of folic acid supplementation in second and third trimester (FASSTT), where significant improvements in cognitive and psychosocial performance were demonstrated in children from mothers supplemented in pregnancy with 400 µg/day FA compared with placebo, we examined methylation patterns from cord blood (CB) using the EPIC array which covers approximately 850,000 cytosine–guanine (CG) sites across the genome. Genes showing significant differences were verified using pyrosequencing and mechanistic approaches used in vitro to determine effects on transcription. RESULTS: FA supplementation resulted in significant differences in methylation, particularly at brain-related genes. Further analysis showed these genes split into two groups. In one group, which included the CES1 gene, methylation changes at the promoters were important for regulating transcription. We also identified a second group which had a characteristic bimodal profile, with low promoter and high gene body (GB) methylation. In the latter, loss of methylation in the GB is linked to decreases in transcription: this group included the PRKAR1B/HEATR2 genes and the dopamine receptor regulator PDE4C. Overall, methylation in CB also showed good correlation with methylation profiles seen in a published data set of late gestation foetal brain samples. CONCLUSION: We show here clear alterations in DNA methylation at specific classes of neurodevelopmental genes in the same cohort of children, born to FA-supplemented mothers, who previously showed improved cognitive and psychosocial performance. Our results show measurable differences at neural genes which are important for transcriptional regulation and add to the supporting evidence for continued FA supplementation throughout later gestation. This trial was registered on 15 May 2013 at www.isrctn.com as ISRCTN19917787. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-022-01282-y.
format Online
Article
Text
id pubmed-9112484
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-91124842022-05-18 Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms Ondičová, Miroslava Irwin, Rachelle E. Thursby, Sara-Jayne Hilman, Luke Caffrey, Aoife Cassidy, Tony McLaughlin, Marian Lees-Murdock, Diane J. Ward, Mary Murphy, Michelle Lamers, Yvonne Pentieva, Kristina McNulty, Helene Walsh, Colum P. Clin Epigenetics Research BACKGROUND: We previously showed that continued folic acid (FA) supplementation beyond the first trimester of pregnancy appears to have beneficial effects on neurocognitive performance in children followed for up to 11 years, but the biological mechanism for this effect has remained unclear. Using samples from our randomized controlled trial of folic acid supplementation in second and third trimester (FASSTT), where significant improvements in cognitive and psychosocial performance were demonstrated in children from mothers supplemented in pregnancy with 400 µg/day FA compared with placebo, we examined methylation patterns from cord blood (CB) using the EPIC array which covers approximately 850,000 cytosine–guanine (CG) sites across the genome. Genes showing significant differences were verified using pyrosequencing and mechanistic approaches used in vitro to determine effects on transcription. RESULTS: FA supplementation resulted in significant differences in methylation, particularly at brain-related genes. Further analysis showed these genes split into two groups. In one group, which included the CES1 gene, methylation changes at the promoters were important for regulating transcription. We also identified a second group which had a characteristic bimodal profile, with low promoter and high gene body (GB) methylation. In the latter, loss of methylation in the GB is linked to decreases in transcription: this group included the PRKAR1B/HEATR2 genes and the dopamine receptor regulator PDE4C. Overall, methylation in CB also showed good correlation with methylation profiles seen in a published data set of late gestation foetal brain samples. CONCLUSION: We show here clear alterations in DNA methylation at specific classes of neurodevelopmental genes in the same cohort of children, born to FA-supplemented mothers, who previously showed improved cognitive and psychosocial performance. Our results show measurable differences at neural genes which are important for transcriptional regulation and add to the supporting evidence for continued FA supplementation throughout later gestation. This trial was registered on 15 May 2013 at www.isrctn.com as ISRCTN19917787. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-022-01282-y. BioMed Central 2022-05-16 /pmc/articles/PMC9112484/ /pubmed/35578268 http://dx.doi.org/10.1186/s13148-022-01282-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ondičová, Miroslava
Irwin, Rachelle E.
Thursby, Sara-Jayne
Hilman, Luke
Caffrey, Aoife
Cassidy, Tony
McLaughlin, Marian
Lees-Murdock, Diane J.
Ward, Mary
Murphy, Michelle
Lamers, Yvonne
Pentieva, Kristina
McNulty, Helene
Walsh, Colum P.
Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms
title Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms
title_full Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms
title_fullStr Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms
title_full_unstemmed Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms
title_short Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms
title_sort folic acid intervention during pregnancy alters dna methylation, affecting neural target genes through two distinct mechanisms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112484/
https://www.ncbi.nlm.nih.gov/pubmed/35578268
http://dx.doi.org/10.1186/s13148-022-01282-y
work_keys_str_mv AT ondicovamiroslava folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT irwinrachellee folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT thursbysarajayne folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT hilmanluke folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT caffreyaoife folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT cassidytony folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT mclaughlinmarian folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT leesmurdockdianej folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT wardmary folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT murphymichelle folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT lamersyvonne folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT pentievakristina folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT mcnultyhelene folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms
AT walshcolump folicacidinterventionduringpregnancyaltersdnamethylationaffectingneuraltargetgenesthroughtwodistinctmechanisms