Genetic and functional evidence relates a missense variant in B4GALT1 to lower LDL-C and fibrinogen
May E. MontasseriD, Cristopher V. Van HoutiD, Rebecca J. McFarlandiD, Avraham Rosenberg, Myrasol B. Callaway, Biao SheniD, Ning LiiD, Thomas J. DalyiD, Alicia D. HowardiD, Wei LiniD, Yuan MaoiD, Bin YeiD, Giusy Della GattaiD, Gannie TzonevaiD, James A. PerryiD, Kathleen A. RyaniD, Lawrence Miloscio, Aris N. EconomidesiD, NHLBI TOPMed Program, Carole Sztalryd, Braxton D. MitchelliD, Matthew D. HealyiD, Elizabeth A. StreeteniD, Norann A. ZaghlouliD, Simeon I. TayloriD, , Alan R. ShuldineriD
Abstract
Increased LDL-cholesterol (LDL-C) and fibrinogen are independent risk factors for cardiovascular disease (CVD). We identified novel associations between an Amish-enriched missense variant (p.Asn352Ser) in a functional domain of beta-1,4-galactosyltransferase 1 (B4GALT1) and 13.5 mg/dl lower LDL-C (p=1.6E-15), and 26 mg/dl lower plasma fibrinogen (p= 9.8E-05). N-linked glycan profiling found p.Asn352Ser to be associated (p-values from 1.4E-06 to 1.0E-17) with decreased glycosylation of glycoproteins including: fibrinogen, ApoB100, immunoglobulin G (IgG), and transferrin. In vitro assays found that the mutant (352Ser) protein had 50% lower galactosyltransferase activity compared to wild type (352Asn) protein. Knockdown of b4galt1 in zebrafish embryos resulted in significantly lower LDL-C compared to control, which was fully rescued by co-expression of 352Asn human B4GALT1 mRNA but only partially rescued by co-expression of 352Ser human B4GALT1 mRNA. Our findings establish B4GALT1 as a novel gene associated with lower LDL-C and fibrinogen and suggest that targeted modulation of protein glycosylation may represent a therapeutic approach to decrease CVD risk.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 3
- Organism
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- ADAR RNA editing for cardiovascular disease: Targeting B4GALT1 to modulate lipid metabolism through reduced galactosyltransferase activity
Francesco De Chiara, Eva Coll-de la Rubia, … Gerard J. Platenburg·Molecular Therapy — Nucleic AcidsPeer-reviewed·Jul 9, 2026
- A common polymorphism that protects from cardiovascular disease increases fibronectin processing and secretion
S. Soubeyrand, P. Lau, … R. McPherson·Circulation: Genomic and Precision MedicinePeer-reviewed·Apr 1, 2022
- Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease
Jonas Bille Nielsen, Oren Rom, … Y. Eugene Chen·bioRxiv·Apr 2, 2019
- Novel protein-altering variants associated with serum apolipoprotein and lipid levels
Niina Sandholm, Ronja Hotakainen, … on behalf of the FinnDiane Study Group·Genome MedicinePeer-reviewed·Nov 23, 2022
- A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia
Aiqiu Wei, Yangyang Wu, … Faquan Lin·bioRxiv·Jan 29, 2020
- Hepatic Inactivation of Carnitine Palmitoyltransferase 1a Lowers Apolipoprotein B Containing Lipoproteins in Mice
Robert Nathaniel Helsley, Mikala M. Zelows, … Gregory A. Graf·Arteriosclerosis Thrombosis and Vascular BiologyPeer-reviewed·Jun 12, 2025