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Genetic regulation of post-translational modification of two distinct proteins.

Authors :
Landini A
Trbojević-Akmačić I
Navarro P
Tsepilov YA
Sharapov SZ
Vučković F
Polašek O
Hayward C
Petrović T
Vilaj M
Aulchenko YS
Lauc G
Wilson JF
Klarić L
Source :
Nature communications [Nat Commun] 2022 Mar 24; Vol. 13 (1), pp. 1586. Date of Electronic Publication: 2022 Mar 24.
Publication Year :
2022

Abstract

Post-translational modifications diversify protein functions and dynamically coordinate their signalling networks, influencing most aspects of cell physiology. Nevertheless, their genetic regulation or influence on complex traits is not fully understood. Here, we compare the genetic regulation of the same PTM of two proteins - glycosylation of transferrin and immunoglobulin G (IgG). By performing genome-wide association analysis of transferrin glycosylation, we identify 10 significantly associated loci, 9 of which were not reported previously. Comparing these with IgG glycosylation-associated genes, we note protein-specific associations with genes encoding glycosylation enzymes (transferrin - MGAT5, ST3GAL4, B3GAT1; IgG - MGAT3, ST6GAL1), as well as shared associations (FUT6, FUT8). Colocalisation analyses of the latter suggest that different causal variants in the FUT genes regulate fucosylation of the two proteins. Glycosylation of these proteins is thus genetically regulated by both shared and protein-specific mechanisms.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
35332118
Full Text :
https://doi.org/10.1038/s41467-022-29189-5