Journal
CIRCULATION-GENOMIC AND PRECISION MEDICINE
Volume 15, Issue 2, Pages 121-130Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGEN.121.003428
Keywords
Fibronectin 1; coronary artery disease; Single nucleotide polymorphism; signal peptide; glycosylation
Funding
- Canadian Institutes for Health Research Foundation [154308]
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This study analyzed public databases and used bioinformatic analysis and cell models to validate the association between common genetic variants within the FN1 gene and coronary artery disease risk. The findings showed that higher levels of FN1 protein in plasma were associated with lower coronary artery disease risk, and the L15Q polymorphism in the FN1 signal peptide affected protein secretion and glycosylation.
Background: Fibronectin (FN1) is an essential regulator of homodynamic processes and tissue remodeling that have been proposed to contribute to atherosclerosis. Moreover, recent large-scale genome-wide association studies (GWAS) have linked common genetic variants within the FN1 gene to coronary artery disease risk. Methods: Public databases were analyzed by 2-Sample Mendelian Randomization. Expression constructs encoding short FN1 reporter constructs and full-length plasma FN1 variants were introduced in various cell models. Secreted and cellular levels were then analyzed and quantified by SDS-PAGE and fluorescence microscopy. Mass spectrometry and glycosylation analyses were performed to probe possible posttranscriptional differences. Results: Bioinformatic analyses revealed that common coronary artery disease risk single nucleotide polymorphisms in the FN1 locus associate with circulating levels of FN1 and that higher FN1 (fibronectin 1) protein levels in plasma are linked to lower coronary artery disease risk. The coronary artery disease-associated FN1 locus encompasses a common polymorphism that translates a L15Q variant situated within the FN1 signal peptide. Introduction of FN1 reporter constructs, differing at position 15, revealed differences in secretion, with the FN1 Q15 variant being less well secreted. Moreover, the L15Q polymorphism was found to alter glycosylation in some cell models but not in human plasma. Conclusions: In addition to providing novel functional evidence implicating FN1 in cardioprotection, these findings demonstrate that a common variant within a secretion signal peptide regulates protein function.
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