The alpha-2A-adrenergic receptor (ADRA2A) modulates susceptibility to Raynaud's syndrome
Tervi, A.; Ramste, M.; Abner, E.; Cheng, P.; Lane, J. M.; Maher, M.; Lammi, V.; Strausz, S.; Nguyen, T.; Docampo, M. L.; Gu, W.; FinnGen, ; Estonian biobank research team, ; Esko, T.; Saxena, R.; Palotie, A.; Ripatti, S.; Sinnott-Armstrong, N.; Daly, M. J.; Rabinovitch, M.; Heckman, C. A.; Quertermous, T.; Jones, S. E.; Ollila, H. M.
Show abstract
Raynauds syndrome is a common dysautonomia where exposure to cold increases the vascular tone of distal arteries causing vasoconstriction and hypoxia, particularly in the extremities. Current treatment options are limited and unspecific. Biological mechanisms leading to the phenotype remain uncharacterized. Using genetic and electronic health record data from the UK Biobank, the Mass-General Brigham Biobank, the Estonian Biobank, and the FinnGen study, we identified 11,358 individuals with a diagnosis of Raynauds syndrome and 1,106,871 population controls. We found eight loci including endothelial nitric oxide synthase (NOS3), HLA, and a notable association at the 2A-adrenergic receptor (ADRA2A) locus (rs7090046, P = 3.93x10-47), implicating adrenergic signaling as a major risk factor with Raynauds syndrome. We further investigate the role of the variants and ADRA2A expression in functional and physiological models. In silico follow-up analysis revealed an expression quantitative trait locus (eQTL) that co-localized and increased ADRA2A gene expression in a tissue-specific manner in the distal arteries. Staining with RNA scope further clarified the specificity of ADRA2A expression in small vessels. We show by CRISPR gene editing that the SNP region modifies ADRA2A gene expression in pulmonary artery smooth muscle cells. Finally, we performed a functional contraction assay on smooth muscle cells in cold conditions and showed lower contraction in ADRA2A-deficient and higher contraction in ADRA2A-overexpressing smooth muscle cells. Our results indicate that Raynauds syndrome is related to vascular function mediated by adrenergic signaling through ADRA2A. Our study highlights the power of genome-wide association testing as a discovery tool for poorly understood clinical endpoints and further clarifies the role of adrenergic signaling in Raynauds syndrome by fine-mapping, using in vitro genomic manipulations and functional validation in distal smooth muscle cell populations located in arterioles
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity 96%
- Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertension 96%
- Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs 96%
Similar papers in this journal
- Central role of glycosylation processes in human genetic susceptibility to SARS-CoV-2 infections with Omicron variants 97%
- Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease 97%
- Deep learning enables genetic analysis of the human thoracic aorta 96%
Similar papers in this journal
- Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy 96%
- Association between genes regulating neural pathways for quantitative traits of speech and language disorders 92%
- Discordance between a deep learning model and clinical-grade variant pathogenicity classification in a rare disease cohort 92%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.