Genetic-epigenetic dysregulation of thymic TSH receptor gene expression triggers thyroid autoimmunity.
Ontology highlight
ABSTRACT: Graves disease (GD) is an autoimmune condition caused by interacting genetic and environmental factors. Genetic studies have mapped several single-nucleotide polymorphisms (SNPs) that are strongly associated with GD, but the mechanisms by which they trigger disease are unknown. We hypothesized that epigenetic modifications induced by microenvironmental influences of cytokines can reveal the functionality of GD-associated SNPs. We analyzed genome-wide histone H3 lysine 4 methylation and gene expression in thyroid cells induced by IFNα, a key cytokine secreted during viral infections, and overlapped them with known GD-associated SNPs. We mapped an open chromatin region overlapping two adjacent GD-associated SNPs (rs12101255 and rs12101261) in intron 1 of the thyroid stimulating hormone recep
SUBMITTER: Stefan M
PROVIDER: S-EPMC4151767 | biostudies-literature | 2014 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA