Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature

Primary Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by lymphocytic infiltration and damage of exocrine salivary and lacrimal glands. The etiology of SS is complex with environmental triggers and genetic factors involved. By conducting an integrated multi-omics study, we co...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Teruel Maria
Barturen Guillermo
Martinez-Bueno Manuel
Castellini-Pérez Olivia
Barroso-Gil Miguel
Povedano Elena
Kerick Martin
Català‑Moll Francesc
PRECISESADS Clinical Consortium
PRECISESADS Flow Cytometry Study Group
Kovács László
Balog Attila
Deák Magdolna
Bocskai Márta
Dulic Sonja
Kádár Gabriella
Dokumentumtípus: Cikk
Megjelent: 2021
Sorozat:SCIENTIFIC REPORTS 11 No. 1
doi:10.1038/s41598-021-01324-0

mtmt:32575652
Online Access:http://publicatio.bibl.u-szeged.hu/23640
Leíró adatok
Tartalmi kivonat:Primary Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by lymphocytic infiltration and damage of exocrine salivary and lacrimal glands. The etiology of SS is complex with environmental triggers and genetic factors involved. By conducting an integrated multi-omics study, we confirmed a vast coordinated hypomethylation and overexpression effects in IFN-related genes, what is known as the IFN signature. Stratified and conditional analyses suggest a strong interaction between SS-associated HLA genetic variation and the presence of Anti-Ro/SSA autoantibodies in driving the IFN epigenetic signature and determining SS. We report a novel epigenetic signature characterized by increased DNA methylation levels in a large number of genes enriched in pathways such as collagen metabolism and extracellular matrix organization. We identified potential new genetic variants associated with SS that might mediate their risk by altering DNA methylation or gene expression patterns, as well as disease-interacting genetic variants that exhibit regulatory function only in the SS population. Our study sheds new light on the interaction between genetics, autoantibody profiles, DNA methylation and gene expression in SS, and contributes to elucidate the genetic architecture of gene regulation in an autoimmune population. © 2021, The Author(s).
Terjedelem/Fizikai jellemzők:Terjedelem: 18 p-Azonosító: 23292
ISSN:2045-2322