Mapping of the gene network that regulates glycan clock of ageing

Abstract: Glycans are an essential structural component of immunoglobulin G (IgG) that modulate its structure and function. However, regulatory mechanisms behind this complex posttranslational modification are not well known. Previous genome-wide association studies (GWAS) identified 29 genomic regions involved in regulation of IgG glycosylation, but only a few were functionally validated. One of the key functional features of IgG glycosylation is the addition of galactose (galactosylation), a trait which was shown to be associated with ageing. We performed GWAS of IgG galactosylation (N=13,705) and identified 16 significantly associated loci, indicating that IgG galactosylation is regulated by a complex network of genes that extends beyond the galactosyltransferase enzyme that adds galactose to IgG glycans. Gene prioritization identified 37 candidate genes. Using a recently developed CRISPR/dCas9 system we manipulated gene expression of candidate genes in the in vitro IgG expression system. Upregulation of three genes, EEF1A1, MANBA and TNFRSF13B, changed the IgG glycome composition, which confirmed that these three genes are involved in IgG galactosylation in this in vitro expression system

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
Aging. - 15, 24 (2023) , 14509-14552, ISSN: 1945-4589

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2024
Creator
Frkatović-Hodžić, Azra
Mijakovac, Anika
Miškec, Karlo
Li, Yong
Köttgen, Anna
Klarić, Lucija
Zoldoš, Vlatka
Lauc, Gordan

DOI
10.18632/aging.205106
URN
urn:nbn:de:bsz:25-freidok-2426671
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:48 PM CET

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Associated

Time of origin

  • 2024

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