SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:prod.swepub.kib.ki.se:148350783"
 

Search: onr:"swepub:oai:prod.swepub.kib.ki.se:148350783" > Integrative epigeno...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

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

Teruel, M (author)
Barturen, G (author)
Martinez-Bueno, M (author)
show more...
Castellini-Perez, O (author)
Barroso-Gil, M (author)
Povedano, E (author)
Kerick, M (author)
Catala-Moll, F (author)
Makowska, Z (author)
Buttgereit, A (author)
Pers, JO (author)
Maranon, C (author)
Ballestar, E (author)
Martin, J (author)
Carnero-Montoro, E (author)
Alarcon-Riquelme, ME (author)
Karolinska Institutet
show less...
 (creator_code:org_t)
2021-12-02
2021
English.
In: Scientific reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 11:1, s. 23292-
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • 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.

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view