RAMEN: Dissecting individual, additive and interactive gene-environment contributions to DNA methylome variability in cord blood
Erick I. Navarro‐DelgadoiD, Darina CzamaraiD, Karlie EdwardsiD, Maggie P. FuiD, Sarah M. MerrilliD, Chaini KonwariD, Julie L. MacIsaac, David T S LiniD, Piush J. MandhaneiD, Elinor SimonsiD, Padmaja SubbaraoiD, Theo J. MoraesiD, Jari M. T. LahtiiD, Gregory E. MilleriD, Elisabeth B. BinderiD, Katri RäikköneniD, Stuart E. TurveyiD, Keegan D. KorthaueriD, Michael Steffen KoboriD
Abstract
DNA methylation (DNAme) is the most commonly studied epigenetic mark in human populations. DNAme has gained attention in the Developmental Origins of Health and Disease field due to its gene expression regulation and potential long-term stability. Genetic variation and environmental exposures are amongst the main factors influencing inter-individual DNAme variability. However, the proportion and genomic distribution of their individual, additive and interactive effects on the DNA methylome remains unclear. Here, we introduce RAMEN, a Findable, Accessible, Interoperable, and Reusable (FAIR) framework tailored for DNAme microarrays. Using machine learning and statistical techniques, RAMEN models and dissects gene-environment contributions to genome-wide Variably Methylated Regions (VMRs), while controlling for spurious associations. To comprehensively test the power of RAMEN, we analyzed and characterized VMRs from cord blood samples from two independent cohorts (CHILD and PREDO; overall n=1,662). We identified genetics as a consistent key contributor to DNAme variability, usually in additive and interactive combinations with the environment, with genetic terms explaining the largest proportion of DNAme variance, compared to environmental and interaction terms. Operationalizing RAMEN as an R package to conduct scalable genome-exposome contribution analyses, our results highlighted the importance of genetic variation in sculpting DNAme patterns in early life.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- FWCI
- 0.30
- Field percentile
- 46th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Variably methylated regions in the newborn epigenome: environmental, genetic and combined influences
Darina Czamara, Gökçen Eraslan, … Robert M. Maier·Nature CommunicationsPeer-reviewed·Jun 11, 2019
- A survey of DNA methylation polymorphism identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome
Paras Garg, Ricky S. Joshi, … Andrew J. Sharp·bioRxiv·Sep 15, 2017
- Longitudinal data reveal strong genetic and weak non-genetic components of ethnicity-dependent blood DNA methylation levels
Chris G. McKennan, Katherine A. Naughton, … Carole Ober·EpigeneticsPeer-reviewed·Sep 30, 2020
- Epigenome-wide contributions to individual differences in childhood phenotypes: A GREML approach
Alexander Neumann, Jean‐Baptiste Pingault, … Esther Walton·Clinical EpigeneticsPeer-reviewed·Apr 19, 2022
- Children's DNA Methylation and Family Dynamics in a Congo Basin Subsistence Community: Links with Parental Conflict and Fathers' Caregiving
Meingold Hiu-ming Chan, Sarah M. Merrill, … Lee T. Gettler·bioRxiv·Jun 19, 2026
- Genetic impacts on within-pair DNA methylation variance in monozygotic twins capture gene-environment interactions and cell-type effects
Xiaopu Zhang, İdil Yet, … Jordana T. Bell·Genome biologyPeer-reviewed·Feb 7, 2026