The University of Southampton
University of Southampton Institutional Repository

The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes

The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes
The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes
Integrating the genotype with epigenetic marks holds the promise of better understanding the biology that underlies the complex interactions of inherited and environmental components that define the developmental origins of a range of disorders. The quality of the in utero environment significantly influences health over the lifecourse. Epigenetics, and in particular DNA methylation marks, have been postulated as a mechanism for the enduring effects of the prenatal environment. Accordingly, neonate methylomes contain molecular memory of the individual in utero experience. However, interindividual variation in methylation can also be a consequence of DNA sequence polymorphisms that result in methylation quantitative trait loci (methQTLs) and, potentially, the interaction between fixed genetic variation and environmental influences. We surveyed the genotypes and DNA methylomes of 237 neonates and found 1423 punctuate regions of the methylome that were highly variable across individuals, termed variably methylated regions (VMRs), against a backdrop of homogeneity. MethQTLs were readily detected in neonatal methylomes, and genotype alone best explained ?25% of the VMRs. We found that the best explanation for 75% of VMRs was the interaction of genotype with different in utero environments, including maternal smoking, maternal depression, maternal BMI, infant birth weight, gestational age, and birth order. Our study sheds new light on the complex relationship between biological inheritance as represented by genotype and individual prenatal experience and suggests the importance of considering both fixed genetic variation and environmental factors in interpreting epigenetic variation.
1088-9051
1064-1074
Teh, Ai Ling
af437ef4-60d8-4b1f-9c3c-54ab35a1ac23
Pan, Hong
89ffb703-039c-4adc-9de9-1a125d3b2cf1
Chen, Li
63e9dd39-9be1-4416-82cb-58efdc1b23c1
Ong, Mei-Lyn
f5580640-95e1-4da7-9295-5c498dba6497
Dogra, Shaillay
5b21d189-6557-416a-bebc-46c21f01e8c4
Wong, Johnny
27dad71e-fa49-4f36-a479-e0788e2be082
MacIsaac, Julia L.
4e74f97f-0016-4bfd-9154-25fa22e2a4b6
Mah, Sarah M.
c2e42794-1102-4b9c-99f3-fab395cb34c4
McEwen, Lisa M
2282d9cd-22f9-4ed5-9020-15691d677e65
Saw, Seang-Mei
54ff7be9-beda-4b86-b4db-9168b142e53b
Godfrey, K.M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Chong, Yap-Seng
7043124b-e892-4d4b-8bb7-6d35ed94e136
Kwek, Kenneth
020d4ba4-4abe-4d07-84ec-b7787d94277d
Kwoh, Chee-Keong
53e2ca31-fa76-4c35-89ad-86aa4011e538
Soh, Shu-E.
acd6791d-fbf2-4ec7-a1f5-7bb539f44049
Chong, Mary F.F.
1e188259-b1ab-4448-9e65-5b6a0fd99502
Barton, Sheila
4f674382-ca0b-44ad-9670-e71a0b134ef0
Karnani, Neerja
f4d4879d-3be1-4d6d-8d37-48af1035a4cf
Cheong, Clara Y.
496f5ebb-1dfb-47f4-abae-08d323ddefc4
Buschdorf, Jan Paul
17b01845-8b05-4179-b3a7-86a4c9167724
Stünkel, Walter
13f2d009-099e-4982-b19f-5d0bbe016251
Kobor, Michael S.
e387ab6f-d060-4d39-95c6-acf0c3b9687b
Meaney, Michael J.
5c6db45a-1f5b-4e1f-8c0b-07a8f7b29f66
Gluckman, P.D.
492295c0-ef71-4871-ad5a-771c98e1059a
Holbrook, Joanna D.
9188a129-7683-4e86-92bc-5dc2d41ac91b
Teh, Ai Ling
af437ef4-60d8-4b1f-9c3c-54ab35a1ac23
Pan, Hong
89ffb703-039c-4adc-9de9-1a125d3b2cf1
Chen, Li
63e9dd39-9be1-4416-82cb-58efdc1b23c1
Ong, Mei-Lyn
f5580640-95e1-4da7-9295-5c498dba6497
Dogra, Shaillay
5b21d189-6557-416a-bebc-46c21f01e8c4
Wong, Johnny
27dad71e-fa49-4f36-a479-e0788e2be082
MacIsaac, Julia L.
4e74f97f-0016-4bfd-9154-25fa22e2a4b6
Mah, Sarah M.
c2e42794-1102-4b9c-99f3-fab395cb34c4
McEwen, Lisa M
2282d9cd-22f9-4ed5-9020-15691d677e65
Saw, Seang-Mei
54ff7be9-beda-4b86-b4db-9168b142e53b
Godfrey, K.M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Chong, Yap-Seng
7043124b-e892-4d4b-8bb7-6d35ed94e136
Kwek, Kenneth
020d4ba4-4abe-4d07-84ec-b7787d94277d
Kwoh, Chee-Keong
53e2ca31-fa76-4c35-89ad-86aa4011e538
Soh, Shu-E.
acd6791d-fbf2-4ec7-a1f5-7bb539f44049
Chong, Mary F.F.
1e188259-b1ab-4448-9e65-5b6a0fd99502
Barton, Sheila
4f674382-ca0b-44ad-9670-e71a0b134ef0
Karnani, Neerja
f4d4879d-3be1-4d6d-8d37-48af1035a4cf
Cheong, Clara Y.
496f5ebb-1dfb-47f4-abae-08d323ddefc4
Buschdorf, Jan Paul
17b01845-8b05-4179-b3a7-86a4c9167724
Stünkel, Walter
13f2d009-099e-4982-b19f-5d0bbe016251
Kobor, Michael S.
e387ab6f-d060-4d39-95c6-acf0c3b9687b
Meaney, Michael J.
5c6db45a-1f5b-4e1f-8c0b-07a8f7b29f66
Gluckman, P.D.
492295c0-ef71-4871-ad5a-771c98e1059a
Holbrook, Joanna D.
9188a129-7683-4e86-92bc-5dc2d41ac91b

Teh, Ai Ling, Pan, Hong, Chen, Li, Ong, Mei-Lyn, Dogra, Shaillay, Wong, Johnny, MacIsaac, Julia L., Mah, Sarah M., McEwen, Lisa M, Saw, Seang-Mei, Godfrey, K.M., Chong, Yap-Seng, Kwek, Kenneth, Kwoh, Chee-Keong, Soh, Shu-E., Chong, Mary F.F., Barton, Sheila, Karnani, Neerja, Cheong, Clara Y., Buschdorf, Jan Paul, Stünkel, Walter, Kobor, Michael S., Meaney, Michael J., Gluckman, P.D. and Holbrook, Joanna D. (2014) The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes. Genome Research, 24 (7), 1064-1074. (doi:10.1101/gr.171439.113). (PMID:8090226)

Record type: Article

Abstract

Integrating the genotype with epigenetic marks holds the promise of better understanding the biology that underlies the complex interactions of inherited and environmental components that define the developmental origins of a range of disorders. The quality of the in utero environment significantly influences health over the lifecourse. Epigenetics, and in particular DNA methylation marks, have been postulated as a mechanism for the enduring effects of the prenatal environment. Accordingly, neonate methylomes contain molecular memory of the individual in utero experience. However, interindividual variation in methylation can also be a consequence of DNA sequence polymorphisms that result in methylation quantitative trait loci (methQTLs) and, potentially, the interaction between fixed genetic variation and environmental influences. We surveyed the genotypes and DNA methylomes of 237 neonates and found 1423 punctuate regions of the methylome that were highly variable across individuals, termed variably methylated regions (VMRs), against a backdrop of homogeneity. MethQTLs were readily detected in neonatal methylomes, and genotype alone best explained ?25% of the VMRs. We found that the best explanation for 75% of VMRs was the interaction of genotype with different in utero environments, including maternal smoking, maternal depression, maternal BMI, infant birth weight, gestational age, and birth order. Our study sheds new light on the complex relationship between biological inheritance as represented by genotype and individual prenatal experience and suggests the importance of considering both fixed genetic variation and environmental factors in interpreting epigenetic variation.

Text
Genome Res.-2014-Teh-1064-74.pdf - Version of Record
Available under License Other.
Download (1MB)

More information

e-pub ahead of print date: 7 April 2014
Published date: July 2014
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 367373
URI: http://eprints.soton.ac.uk/id/eprint/367373
ISSN: 1088-9051
PURE UUID: 1869cd65-26d3-409f-b84c-152662b616ca
ORCID for K.M. Godfrey: ORCID iD orcid.org/0000-0002-4643-0618
ORCID for Sheila Barton: ORCID iD orcid.org/0000-0003-4963-4242

Catalogue record

Date deposited: 22 Aug 2014 14:50
Last modified: 15 Mar 2024 03:10

Export record

Altmetrics

Contributors

Author: Ai Ling Teh
Author: Hong Pan
Author: Li Chen
Author: Mei-Lyn Ong
Author: Shaillay Dogra
Author: Johnny Wong
Author: Julia L. MacIsaac
Author: Sarah M. Mah
Author: Lisa M McEwen
Author: Seang-Mei Saw
Author: K.M. Godfrey ORCID iD
Author: Yap-Seng Chong
Author: Kenneth Kwek
Author: Chee-Keong Kwoh
Author: Shu-E. Soh
Author: Mary F.F. Chong
Author: Sheila Barton ORCID iD
Author: Neerja Karnani
Author: Clara Y. Cheong
Author: Jan Paul Buschdorf
Author: Walter Stünkel
Author: Michael S. Kobor
Author: Michael J. Meaney
Author: P.D. Gluckman
Author: Joanna D. Holbrook

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.

×