Expression patterns common and unique to ulcerative colitis and celiac disease

Autoimmune diseases like celiac disease (CeD) and ulcerative colitis (UC) show a common genetic background defined by the existence of shared susceptibility loci. We aimed to go deeper into this common genetic background through performing a cross‐disease study based on gene expression. We measured...

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Veröffentlicht in:Annals of human genetics 2019-03, Vol.83 (2), p.86-94
Hauptverfasser: Medrano, Luz María, Pascual, Virginia, Bodas, Andrés, López‐Palacios, Natalia, Salazar, Isabel, Espino‐Paisán, Laura, González‐Pérez, Beatriz, Urcelay, Elena, Mendoza, Juan Luis, Núñez, Concepción
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Sprache:eng
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Zusammenfassung:Autoimmune diseases like celiac disease (CeD) and ulcerative colitis (UC) show a common genetic background defined by the existence of shared susceptibility loci. We aimed to go deeper into this common genetic background through performing a cross‐disease study based on gene expression. We measured the expression of 21 genes located in 13 CeD‐UC susceptibility regions, and 10 genes in five CeD risk regions. Determinations were carried out in colon/rectum samples from 13 UC patients (inflamed and uninflamed tissue) and four colon samples from controls. Duodenal samples from 19 CeD patients and 12 controls were used for comparisons. Differences were analyzed using the Bayesian method. The shared chromosomal regions containing TNFAIP3, PTPN2, ICOSLG, C1orf106, and IL21 showed similar results in both diseases. FASLG, PLEK, CCR4, and TAGAP, all located in CeD risk loci, were up‐regulated in both CeD and UC patients. Finally, ZFP36L1, ZMIZ1, PUS10, UBE2L3, and BACH2 showed opposite results in CeD and UC. A high complexity underlies autoimmune common susceptibility loci, as the expression pattern of the studied genes does not always correlate with the one expected attending to the apparent genetic background. Differentially expressed genes such as ZFP36L1, ZMIZ1, PUS10, and BACH2 deserve further research in autoimmune diseases.
ISSN:0003-4800
1469-1809
DOI:10.1111/ahg.12293