Systemic interindividual DNA methylation variants in cattle share major hallmarks with those in humans.

Bovine CoRSIV Cow DoHAD Systemic interindividual epigenetic variation

Journal

Genome biology
ISSN: 1474-760X
Titre abrégé: Genome Biol
Pays: England
ID NLM: 100960660

Informations de publication

Date de publication:
15 Jul 2024
Historique:
received: 22 09 2023
accepted: 13 06 2024
medline: 15 7 2024
pubmed: 15 7 2024
entrez: 14 7 2024
Statut: epublish

Résumé

We recently identified ~ 10,000 correlated regions of systemic interindividual epigenetic variation (CoRSIVs) in the human genome. These methylation variants are amenable to population studies, as DNA methylation measurements in blood provide information on epigenetic regulation throughout the body. Moreover, establishment of DNA methylation at human CoRSIVs is labile to periconceptional influences such as nutrition. Here, we analyze publicly available whole-genome bisulfite sequencing data on multiple tissues of each of two Holstein cows to determine whether CoRSIVs exist in cattle. Focusing on genomic blocks with ≥ 5 CpGs and a systemic interindividual variation index of at least 20, our approach identifies 217 cattle CoRSIVs, a subset of which we independently validate by bisulfite pyrosequencing. Similar to human CoRSIVs, those in cattle are strongly associated with genetic variation. Also as in humans, we show that establishment of DNA methylation at cattle CoRSIVs is particularly sensitive to early embryonic environment, in the context of embryo culture during assisted reproduction. Our data indicate that CoRSIVs exist in cattle, as in humans, suggesting these systemic epigenetic variants may be common to mammals in general. To the extent that individual epigenetic variation at cattle CoRSIVs affects phenotypic outcomes, assessment of CoRSIV methylation at birth may become an important tool for optimizing agriculturally important traits. Moreover, adjusting embryo culture conditions during assisted reproduction may provide opportunities to tailor agricultural outcomes by engineering CoRSIV methylation profiles.

Sections du résumé

BACKGROUND BACKGROUND
We recently identified ~ 10,000 correlated regions of systemic interindividual epigenetic variation (CoRSIVs) in the human genome. These methylation variants are amenable to population studies, as DNA methylation measurements in blood provide information on epigenetic regulation throughout the body. Moreover, establishment of DNA methylation at human CoRSIVs is labile to periconceptional influences such as nutrition. Here, we analyze publicly available whole-genome bisulfite sequencing data on multiple tissues of each of two Holstein cows to determine whether CoRSIVs exist in cattle.
RESULTS RESULTS
Focusing on genomic blocks with ≥ 5 CpGs and a systemic interindividual variation index of at least 20, our approach identifies 217 cattle CoRSIVs, a subset of which we independently validate by bisulfite pyrosequencing. Similar to human CoRSIVs, those in cattle are strongly associated with genetic variation. Also as in humans, we show that establishment of DNA methylation at cattle CoRSIVs is particularly sensitive to early embryonic environment, in the context of embryo culture during assisted reproduction.
CONCLUSIONS CONCLUSIONS
Our data indicate that CoRSIVs exist in cattle, as in humans, suggesting these systemic epigenetic variants may be common to mammals in general. To the extent that individual epigenetic variation at cattle CoRSIVs affects phenotypic outcomes, assessment of CoRSIV methylation at birth may become an important tool for optimizing agriculturally important traits. Moreover, adjusting embryo culture conditions during assisted reproduction may provide opportunities to tailor agricultural outcomes by engineering CoRSIV methylation profiles.

Identifiants

pubmed: 39004763
doi: 10.1186/s13059-024-03307-6
pii: 10.1186/s13059-024-03307-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

185

Subventions

Organisme : NIDDK NIH HHS
ID : 1R01DK125562
Pays : United States
Organisme : Agricultural Research Service
ID : CRIS 3092-5-001-059
Organisme : College of Agriculture and Life Sciences, Cornell University
ID : Schwartz Research Award

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Wen-Jou Chang (WJ)

Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX, United States.

Maria S Baker (MS)

Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX, United States.

Eleonora Laritsky (E)

Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX, United States.

Chathura J Gunasekara (CJ)

Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX, United States.

Uditha Maduranga (U)

Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX, United States.

Justine C Galliou (JC)

Department of Animal Science, Cornell University, Ithaca, NY, United States.

Joseph W McFadden (JW)

Department of Animal Science, Cornell University, Ithaca, NY, United States.

Jessica R Waltemyer (JR)

Department of Animal Science, Cornell University, Ithaca, NY, United States.

Bruce Berggren-Thomas (B)

Department of Animal Science, Cornell University, Ithaca, NY, United States.

Brianna N Tate (BN)

Department of Animal Science, Cornell University, Ithaca, NY, United States.

Hanxue Zhang (H)

Department of Animal Science, Cornell University, Ithaca, NY, United States.

Benjamin D Rosen (BD)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, Beltsville, MD, United States.

Curtis P Van Tassell (CP)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, Beltsville, MD, United States.

George E Liu (GE)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, Beltsville, MD, United States.

Cristian Coarfa (C)

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States.
Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, United States.

Yi Athena Ren (YA)

Department of Animal Science, Cornell University, Ithaca, NY, United States. yi.a.ren@cornell.edu.

Robert A Waterland (RA)

Department of Pediatrics, USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX, United States. waterland@bcm.edu.
Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, United States. waterland@bcm.edu.

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