Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas

• Published in: Diabetologia 2024-02, Vol.67 (2), p.327-332
• Main Authors: Meulebrouck, Sarah, Scherrer, Victoria, Boutry, Raphaël, Toussaint, Bénédicte, Vaillant, Emmanuel, Dechaume, Aurélie, Loiselle, Hélène, Balkau, Beverley, Charpentier, Guillaume, Franc, Sylvia, Marre, Michel, Baron, Morgane, Vaxillaire, Martine, Derhourhi, Mehdi, Boissel, Mathilde, Froguel, Philippe, Bonnefond, Amélie
• Format: Article
• Language: English
• Subjects: Adipose tissue; Beta cells; Cholesterol; Diabetes; Diabetes mellitus (non-insulin dependent); Exons; Homology; Human Physiology; Insulin secretion; Internal Medicine; Life Sciences; Medicine; Medicine & Public Health; Meta-analysis; Metabolic Diseases; Neonates; Pathogenesis; Pathogenicity; Short Communication; Single-nucleotide polymorphism; Zinc finger proteins
• ISSN: 0012-186X; 1432-0428
• DOI: 10.1007/s00125-023-06035-x

Aims/hypothesis GLIS3 encodes a transcription factor involved in pancreatic beta cell development and function. Rare pathogenic, bi-allelic mutations in GLIS3 cause syndromic neonatal diabetes whereas frequent SNPs at this locus associate with common type 2 diabetes risk. Because rare, functional variants located in other susceptibility genes for type 2 diabetes have already been shown to strongly increase individual risk for common type 2 diabetes, we aimed to investigate the contribution of rare pathogenic GLIS3 variants to type 2 diabetes. Methods GLIS3 was sequenced in 5471 individuals from the Rare Variants Involved in Diabetes and Obesity (RaDiO) study. Variant pathogenicity was assessed following the criteria established by the American College of Medical Genetics and Genomics (ACMG). To address the pathogenic strong criterion number 3 (PS3), we conducted functional investigations of these variants using luciferase assays, focusing on capacity of GLIS family zinc finger 3 (GLIS3) to bind to and activate the INS promoter. The association between rare pathogenic or likely pathogenic (P/LP) variants and type 2 diabetes risk (and other metabolic traits) was then evaluated. A meta-analysis combining association results from RaDiO, the 52K study (43,125 individuals) and the TOPMed study (44,083 individuals) was finally performed. Results Through targeted resequencing of GLIS3 , we identified 105 rare variants that were carried by 395 participants from RaDiO. Among them, 49 variants decreased the activation of the INS promoter. Following ACMG criteria, 18 rare variants were classified as P/LP, showing an enrichment in the last two exons compared with the remaining exons ( p 3.5). The burden of these P/LP variants was strongly higher in individuals with type 2 diabetes ( p =3.0×10 −3 ; OR 3.9 [95% CI 1.4, 12]), whereas adiposity, age at type 2 diabetes diagnosis and cholesterol levels were similar between variant carriers and non-carriers with type 2 diabetes. Interestingly, all carriers with type 2 diabetes were sensitive to oral sulfonylureas. A total of 7 P/LP variants were identified in both 52K and TOPMed studies. The meta-analysis of association studies obtained from RaDiO, 52K and TOPMed showed an enrichment of P/LP GLIS3 variants in individuals with type 2 diabetes ( p =5.6×10 −5 ; OR 2.1 [95% CI 1.4, 2.9]). Conclusions/interpretation Rare P/LP GLIS3 variants do contribute to type 2 diabetes risk. The variants located in the distal par