Enhancer RNA transcription pinpoints functional genetic variants linked to asthma
Bidirectional enhancer RNA (eRNA) transcription is a widespread response to environmental signals and glucocorticoids. We investigated whether single nucleotide polymorphisms (SNPs) within dynamically regulated eRNA-transcribing regions contribute to genetic variation in asthma. Through applying multivariate regression modeling with permutation-based significance thresholding to a large clinical cohort, we identified novel associations between asthma and 35 SNPs located in eRNA-transcribing regions implicated in regulating cellular processes relevant to asthma, including rs258760 (mean allele frequency = 0.34, asthma odds ratio = 0.95; P = 5.04E-03). We show that rs258760 disrupts an active aryl hydrocarbon receptor (AHR) response element linked to transcriptional regulation of the glucocorticoid receptor gene by AHR ligands, which are commonly found in combusted air pollution. The role of rs258760 as a protective variant for asthma was independently validated using UK Biobank data. Our findings establish eRNA signatures as a tool for discovery of functional genetic variants and define a novel association between air pollution, glucocorticoid signaling and asthma.
Authors
- Fabienne Gally (ORCID: https://orcid.org/0000-0003-0503-7411)
- Robin D. Dowell (ORCID: https://orcid.org/0000-0001-7665-9985)
- Lynn Sanford (ORCID: https://orcid.org/0000-0002-1255-556X)
- Arnav Gupta (ORCID: https://orcid.org/0000-0002-7439-8168)
- Ann Chen Wu (ORCID: https://orcid.org/0000-0003-0599-9063)
- Margaret Gruca (ORCID: https://orcid.org/0000-0001-5808-5308)
- Carlos Iribarren (ORCID: https://orcid.org/0000-0001-5622-1839)
- Anthony N. Gerber (ORCID: https://orcid.org/0000-0002-5280-8218)
- Amber Dahlin (ORCID: https://orcid.org/0000-0002-2534-5975)
- Sarah K. Sasse
- Scott T. Weiss
Institutions
- Brigham and Women's Hospital (US)
- University of Colorado Hospital (US)
- Kaiser Permanente (US)
- Harvard University (US)
- University of Colorado Boulder (US)
- National Jewish Health (US)
- Harvard Pilgrim Health Care (US)
- University of Colorado Anschutz Medical Campus (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-03-31
- DOI
- https://doi.org/10.1038/s41467-025-57693-x
- Citations
- 4
- Primary Topic
- IL-33, ST2, and ILC Pathways
- Type
- article
- Field-Weighted Citation Impact
- 3.19
Funders
- National Heart, Lung, and Blood Institute
- National Institute of General Medical Sciences