Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease

<p><strong>Background</strong> Many genome- and epigenome-wide association studies (GWAS and EWAS) and studies of promoter methylation of candidate genes for inflammatory bowel disease (IBD) have demonstrated significant associations between genetic and epigenetic changes and IBD....

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Main Authors: Klasić, M, Markulin, D, Vojta, A, Samaržija, I, Biruš, I, Dobrinić, P, Ventham, N, Trbojević-Akmačić, I, Šimurina, M, Štambuk, J, Razdorov, G, Kennedy, N, Satsangi, J, Dias, A, Pinho, S, Annese, V, Latiano, A, D'Inca, R, IBD Consortium, Lauc, G, Zoldoš, V
Format: Journal article
Language:English
Published: BioMed Central 2018
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author Klasić, M
Markulin, D
Vojta, A
Samaržija, I
Biruš, I
Dobrinić, P
Ventham, N
Trbojević-Akmačić, I
Šimurina, M
Štambuk, J
Razdorov, G
Kennedy, N
Satsangi, J
Dias, A
Pinho, S
Annese, V
Latiano, A
D'Inca, R
IBD Consortium
Lauc, G
Zoldoš, V
author_facet Klasić, M
Markulin, D
Vojta, A
Samaržija, I
Biruš, I
Dobrinić, P
Ventham, N
Trbojević-Akmačić, I
Šimurina, M
Štambuk, J
Razdorov, G
Kennedy, N
Satsangi, J
Dias, A
Pinho, S
Annese, V
Latiano, A
D'Inca, R
IBD Consortium
Lauc, G
Zoldoš, V
author_sort Klasić, M
collection OXFORD
description <p><strong>Background</strong> Many genome- and epigenome-wide association studies (GWAS and EWAS) and studies of promoter methylation of candidate genes for inflammatory bowel disease (IBD) have demonstrated significant associations between genetic and epigenetic changes and IBD. Independent GWA studies have identified genetic variants in the BACH2, IL6ST, LAMB1, IKZF1, and MGAT3 loci to be associated with both IBD and immunoglobulin G (IgG) glycosylation.</p> <p><strong>Methods</strong> Using bisulfite pyrosequencing, we analyzed CpG methylation in promoter regions of these five genes from peripheral blood of several hundred IBD patients and healthy controls (HCs) from two independent cohorts, respectively.</p> <p><strong>Results</strong> We found significant differences in the methylation levels in the MGAT3 and BACH2 genes between both Crohn’s disease and ulcerative colitis when compared to HC. The same pattern of methylation changes was identified for both genes in CD19+ B cells isolated from the whole blood of a subset of the IBD patients. A correlation analysis was performed between the MGAT3 and BACH2 promoter methylation and individual IgG glycans, measured in the same individuals of the two large cohorts. MGAT3 promoter methylation correlated significantly with galactosylation, sialylation, and bisecting GlcNAc on IgG of the same patients, suggesting that activity of the GnT-III enzyme, encoded by this gene, might be altered in IBD. The correlations between the BACH2 promoter methylation and IgG glycans were less obvious, since BACH2 is not a glycosyltransferase and therefore may affect IgG glycosylation only indirectly.</p> <p><strong>Conclusions</strong> Our results suggest that epigenetic deregulation of key glycosylation genes might lead to an increase in pro-inflammatory properties of IgG in IBD through a decrease in galactosylation and sialylation and an increase of bisecting GlcNAc on digalactosylated glycan structures. Finally, we showed that CpG methylation in the promoter of the MGAT3 gene is altered in CD3+ T cells isolated from inflamed mucosa of patients with ulcerative colitis from a third smaller cohort, for which biopsies were available, suggesting a functional role of this glyco-gene in IBD pathogenesis.</p>
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spelling oxford-uuid:473b0d21-2c82-4519-9e84-1e55b43d5a782022-03-26T15:18:51ZPromoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel diseaseJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:473b0d21-2c82-4519-9e84-1e55b43d5a78EnglishSymplectic Elements at OxfordBioMed Central2018Klasić, MMarkulin, DVojta, ASamaržija, IBiruš, IDobrinić, PVentham, NTrbojević-Akmačić, IŠimurina, MŠtambuk, JRazdorov, GKennedy, NSatsangi, JDias, APinho, SAnnese, VLatiano, AD'Inca, RIBD ConsortiumLauc, GZoldoš, V<p><strong>Background</strong> Many genome- and epigenome-wide association studies (GWAS and EWAS) and studies of promoter methylation of candidate genes for inflammatory bowel disease (IBD) have demonstrated significant associations between genetic and epigenetic changes and IBD. Independent GWA studies have identified genetic variants in the BACH2, IL6ST, LAMB1, IKZF1, and MGAT3 loci to be associated with both IBD and immunoglobulin G (IgG) glycosylation.</p> <p><strong>Methods</strong> Using bisulfite pyrosequencing, we analyzed CpG methylation in promoter regions of these five genes from peripheral blood of several hundred IBD patients and healthy controls (HCs) from two independent cohorts, respectively.</p> <p><strong>Results</strong> We found significant differences in the methylation levels in the MGAT3 and BACH2 genes between both Crohn’s disease and ulcerative colitis when compared to HC. The same pattern of methylation changes was identified for both genes in CD19+ B cells isolated from the whole blood of a subset of the IBD patients. A correlation analysis was performed between the MGAT3 and BACH2 promoter methylation and individual IgG glycans, measured in the same individuals of the two large cohorts. MGAT3 promoter methylation correlated significantly with galactosylation, sialylation, and bisecting GlcNAc on IgG of the same patients, suggesting that activity of the GnT-III enzyme, encoded by this gene, might be altered in IBD. The correlations between the BACH2 promoter methylation and IgG glycans were less obvious, since BACH2 is not a glycosyltransferase and therefore may affect IgG glycosylation only indirectly.</p> <p><strong>Conclusions</strong> Our results suggest that epigenetic deregulation of key glycosylation genes might lead to an increase in pro-inflammatory properties of IgG in IBD through a decrease in galactosylation and sialylation and an increase of bisecting GlcNAc on digalactosylated glycan structures. Finally, we showed that CpG methylation in the promoter of the MGAT3 gene is altered in CD3+ T cells isolated from inflamed mucosa of patients with ulcerative colitis from a third smaller cohort, for which biopsies were available, suggesting a functional role of this glyco-gene in IBD pathogenesis.</p>
spellingShingle Klasić, M
Markulin, D
Vojta, A
Samaržija, I
Biruš, I
Dobrinić, P
Ventham, N
Trbojević-Akmačić, I
Šimurina, M
Štambuk, J
Razdorov, G
Kennedy, N
Satsangi, J
Dias, A
Pinho, S
Annese, V
Latiano, A
D'Inca, R
IBD Consortium
Lauc, G
Zoldoš, V
Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease
title Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease
title_full Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease
title_fullStr Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease
title_full_unstemmed Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease
title_short Promoter methylation of the MGAT3 and BACH2 genes correlates with the composition of the immunoglobulin G glycome in inflammatory bowel disease
title_sort promoter methylation of the mgat3 and bach2 genes correlates with the composition of the immunoglobulin g glycome in inflammatory bowel disease
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