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Context-specific eQTLs provide deeper insight into causal genes underlying shared genetic architecture of COVID-19 and idiopathic pulmonary fibrosis.

Publication ,  Journal Article
Dalapati, T; Wang, L; Jones, AG; Cardwell, J; Konigsberg, IR; Bossé, Y; Sin, DD; Timens, W; Hao, K; Yang, I; Ko, DC
Published in: HGG Adv
January 27, 2025

Most genetic variants identified through genome-wide association studies (GWASs) are suspected to be regulatory in nature, but only a small fraction colocalize with expression quantitative trait loci (eQTLs, variants associated with expression of a gene). Therefore, it is hypothesized but largely untested that integration of disease GWAS with context-specific eQTLs will reveal the underlying genes driving disease associations. We used colocalization and transcriptomic analyses to identify shared genetic variants and likely causal genes associated with critically ill COVID-19 and idiopathic pulmonary fibrosis. We first identified five genome-wide significant variants associated with both diseases. Four of the variants did not demonstrate clear colocalization between GWAS and healthy lung eQTL signals. Instead, two of the four variants colocalized only in cell type- and disease-specific eQTL datasets. These analyses pointed to higher ATP11A expression from the C allele of rs12585036, in monocytes and in lung tissue from primarily smokers, which increased risk of idiopathic pulmonary fibrosis (IPF) and decreased risk of critically ill COVID-19. We also found lower DPP9 expression (and higher methylation at a specific CpG) from the G allele of rs12610495, acting in fibroblasts and in IPF lungs, and increased risk of IPF and critically ill COVID-19. We further found differential expression of the identified causal genes in diseased lungs when compared to non-diseased lungs, specifically in epithelial and immune cell types. These findings highlight the power of integrating GWASs, context-specific eQTLs, and transcriptomics of diseased tissue to harness human genetic variation to identify causal genes and where they function during multiple diseases.

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Published In

HGG Adv

DOI

EISSN

2666-2477

Publication Date

January 27, 2025

Volume

6

Issue

2

Start / End Page

100410

Location

United States

Related Subject Headings

  • 3105 Genetics
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Dalapati, T., Wang, L., Jones, A. G., Cardwell, J., Konigsberg, I. R., Bossé, Y., … Ko, D. C. (2025). Context-specific eQTLs provide deeper insight into causal genes underlying shared genetic architecture of COVID-19 and idiopathic pulmonary fibrosis. HGG Adv, 6(2), 100410. https://doi.org/10.1016/j.xhgg.2025.100410
Dalapati, Trisha, Liuyang Wang, Angela G. Jones, Jonathan Cardwell, Iain R. Konigsberg, Yohan Bossé, Don D. Sin, et al. “Context-specific eQTLs provide deeper insight into causal genes underlying shared genetic architecture of COVID-19 and idiopathic pulmonary fibrosis.HGG Adv 6, no. 2 (January 27, 2025): 100410. https://doi.org/10.1016/j.xhgg.2025.100410.
Dalapati T, Wang L, Jones AG, Cardwell J, Konigsberg IR, Bossé Y, et al. Context-specific eQTLs provide deeper insight into causal genes underlying shared genetic architecture of COVID-19 and idiopathic pulmonary fibrosis. HGG Adv. 2025 Jan 27;6(2):100410.
Dalapati, Trisha, et al. “Context-specific eQTLs provide deeper insight into causal genes underlying shared genetic architecture of COVID-19 and idiopathic pulmonary fibrosis.HGG Adv, vol. 6, no. 2, Jan. 2025, p. 100410. Pubmed, doi:10.1016/j.xhgg.2025.100410.
Dalapati T, Wang L, Jones AG, Cardwell J, Konigsberg IR, Bossé Y, Sin DD, Timens W, Hao K, Yang I, Ko DC. Context-specific eQTLs provide deeper insight into causal genes underlying shared genetic architecture of COVID-19 and idiopathic pulmonary fibrosis. HGG Adv. 2025 Jan 27;6(2):100410.

Published In

HGG Adv

DOI

EISSN

2666-2477

Publication Date

January 27, 2025

Volume

6

Issue

2

Start / End Page

100410

Location

United States

Related Subject Headings

  • 3105 Genetics