The University of Southampton
University of Southampton Institutional Repository

Gestational diabetes mellitus placentas exhibit epimutations at placental development genes

Gestational diabetes mellitus placentas exhibit epimutations at placental development genes
Gestational diabetes mellitus placentas exhibit epimutations at placental development genes
Gestational diabetes mellitus (GDM) is a maternal metabolic disorder that perturbs placental development and increases the risk of offspring short- and long-term metabolic disorders. The mechanisms by which GDM impairs placental development remain poorly understood. Here, we defined the DNA methylome of GDM placentas and determined whether GDM perturbs methylation at genes important for placental development. We conducted an epigenome-wide association study of 42 placentas from pregnancies in the South African Soweto First 1000 days cohort (S1000). Using genome-wide bisulfite sequencing, we compared non-GDM placentas to GDM placentas with similar proportions from obese and non-obese mothers. Compared to non-GDM, GDM placentas exhibited a distinct methylation profile consisting of 12,210 differentially methylated CpGs (DMCs) that mapped to 3,875 genes. Epigenetically altered genes were enriched in Wnt and cadherin signalling pathways, both critical in placentation and embryogenesis. We also defined regional DNA methylation perturbation in GDM placentas at 11 placental development genes. These findings reveal extensive changes to the placental epigenome of GDM pregnancies and highlight perturbation enriched at important placental development genes. These molecular changes represent potential mechanisms for GDM-induced placental effects that may serve as candidate biomarkers for placental, maternal, and foetal health. Using a study design that used similar proportions of obese and non-obese mothers in our case and control pregnancies, we minimized the detection of changes due to obesity alone. Further work will be necessary to investigate the extent of the influence of obesity on these GDM-related placental epigenetic changes.
figshare
Xue, Jing
a74dc420-09d8-464f-a88f-16de77f37c89
Ideraabdullah, Folami
2c303209-c0d0-4ab9-b68b-33e6b7cbb16f
Brouwer, Cory
d0af6018-c855-438f-afe1-6b8d31eae81e
Jones, Corbin
6e946ebf-ae72-4f11-84c4-f490d2539406
Adair, Linda
a61f2718-4030-424b-945a-6224ed79ce1b
Gharaibeh, Raad
5c5b94bc-8b17-4dfe-9a9a-ab77bf68ec1c
Norris, Shane A.
1d346f1b-6d5f-4bca-ac87-7589851b75a4
Meyrueix, Laetitia P.
ba971f8e-3bd9-4991-8707-5019d2ccc84e
Xue, Jing
a74dc420-09d8-464f-a88f-16de77f37c89
Ideraabdullah, Folami
2c303209-c0d0-4ab9-b68b-33e6b7cbb16f
Brouwer, Cory
d0af6018-c855-438f-afe1-6b8d31eae81e
Jones, Corbin
6e946ebf-ae72-4f11-84c4-f490d2539406
Adair, Linda
a61f2718-4030-424b-945a-6224ed79ce1b
Gharaibeh, Raad
5c5b94bc-8b17-4dfe-9a9a-ab77bf68ec1c
Norris, Shane A.
1d346f1b-6d5f-4bca-ac87-7589851b75a4
Meyrueix, Laetitia P.
ba971f8e-3bd9-4991-8707-5019d2ccc84e

(2022) Gestational diabetes mellitus placentas exhibit epimutations at placental development genes. figshare doi:10.6084/m9.figshare.20523820 [Dataset]

Record type: Dataset

Abstract

Gestational diabetes mellitus (GDM) is a maternal metabolic disorder that perturbs placental development and increases the risk of offspring short- and long-term metabolic disorders. The mechanisms by which GDM impairs placental development remain poorly understood. Here, we defined the DNA methylome of GDM placentas and determined whether GDM perturbs methylation at genes important for placental development. We conducted an epigenome-wide association study of 42 placentas from pregnancies in the South African Soweto First 1000 days cohort (S1000). Using genome-wide bisulfite sequencing, we compared non-GDM placentas to GDM placentas with similar proportions from obese and non-obese mothers. Compared to non-GDM, GDM placentas exhibited a distinct methylation profile consisting of 12,210 differentially methylated CpGs (DMCs) that mapped to 3,875 genes. Epigenetically altered genes were enriched in Wnt and cadherin signalling pathways, both critical in placentation and embryogenesis. We also defined regional DNA methylation perturbation in GDM placentas at 11 placental development genes. These findings reveal extensive changes to the placental epigenome of GDM pregnancies and highlight perturbation enriched at important placental development genes. These molecular changes represent potential mechanisms for GDM-induced placental effects that may serve as candidate biomarkers for placental, maternal, and foetal health. Using a study design that used similar proportions of obese and non-obese mothers in our case and control pregnancies, we minimized the detection of changes due to obesity alone. Further work will be necessary to investigate the extent of the influence of obesity on these GDM-related placental epigenetic changes.

This record has no associated files available for download.

More information

Published date: 1 January 2022

Identifiers

Local EPrints ID: 472228
URI: http://eprints.soton.ac.uk/id/eprint/472228
PURE UUID: ef51ba7c-1028-4116-ab2a-be70765a5d78
ORCID for Shane A. Norris: ORCID iD orcid.org/0000-0001-7124-3788

Catalogue record

Date deposited: 29 Nov 2022 17:55
Last modified: 24 Jan 2024 02:57

Export record

Altmetrics

Contributors

Contributor: Jing Xue
Contributor: Folami Ideraabdullah
Contributor: Cory Brouwer
Contributor: Corbin Jones
Contributor: Linda Adair
Contributor: Raad Gharaibeh
Contributor: Shane A. Norris ORCID iD
Contributor: Laetitia P. Meyrueix

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×