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Diabetes Risk Loci-associated Pathways Are Shared Across Metabolic Tissues

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2022 May 15
PMID 35568807
Authors
Affiliations
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Abstract

Aims/hypothesis: Numerous genome-wide association studies have been performed to understand the influence of genetic variation on type 2 diabetes etiology. Many identified risk variants are located in non-coding and intergenic regions, which complicates understanding of how genes and their downstream pathways are influenced. An integrative data approach will help to understand the mechanism and consequences of identified risk variants.

Methods: In the current study we use our previously developed method CONQUER to overlap 403 type 2 diabetes risk variants with regulatory, expression and protein data to identify tissue-shared disease-relevant mechanisms.

Results: One SNP rs474513 was found to be an expression-, protein- and metabolite QTL. Rs474513 influenced LPA mRNA and protein levels in the pancreas and plasma, respectively. On the pathway level, in investigated tissues most SNPs linked to metabolism. However, in eleven of the twelve tissues investigated nine SNPs were linked to differential expression of the ribosome pathway. Furthermore, seven SNPs were linked to altered expression of genes linked to the immune system. Among them, rs601945 was found to influence multiple HLA genes, including HLA-DQA2, in all twelve tissues investigated.

Conclusion: Our results show that in addition to the classical metabolism pathways, other pathways may be important to type 2 diabetes that show a potential overlap with type 1 diabetes.

Citing Articles

gsQTL: Associating genetic risk variants with gene sets by exploiting their shared variability.

Bouland G, Tesi N, Mahfouz A, Reinders M bioRxiv. 2024; .

PMID: 39345521 PMC: 11429704. DOI: 10.1101/2024.09.13.612853.

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