A comprehensive map of human glucokinase variant activity

• Published in: Genome Biology Vol. 24; no. 1; pp. 97 - 23
• Main Authors: Gersing, Sarah, Cagiada, Matteo, Gebbia, Marinella, Gjesing, Anette P, Coté, Atina G, Seesankar, Gireesh, Li, Roujia, Tabet, Daniel, Weile, Jochen, Stein, Amelie, Gloyn, Anna L, Hansen, Torben, Roth, Frederick P, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus
• Format: Journal Article
• Language: English
• Published: England BioMed Central 26.04.2023; BMC
• Subjects: Catalysis; Complementation; Conformation; Deep mutational scanning; Diabetes; Diabetes mellitus; Diabetes Mellitus, Type 2 - diagnosis; Diabetes Mellitus, Type 2 - genetics; Drug development; Evolutionary conservation; Fasting; Genetic screening; Genetic Testing; Glucokinase; Glucokinase - chemistry; Glucokinase - genetics; Glucose; Humans; Hyperglycemia; Hypoglycemia; Insulin; Insulin secretion; Libraries; Mutation; Mutation, Missense; Phosphorylation; Surveillance; Variants of uncertain significance; Deep mutational scanning; Variants of uncertain significance; Diabetes
• ISSN: 1474-760X; 1474-7596; 1474-760X
• DOI: 10.1186/s13059-023-02935-8

Glucokinase (GCK) regulates insulin secretion to maintain appropriate blood glucose levels. Sequence variants can alter GCK activity to cause hyperinsulinemic hypoglycemia or hyperglycemia associated with GCK-maturity-onset diabetes of the young (GCK-MODY), collectively affecting up to 10 million people worldwide. Patients with GCK-MODY are frequently misdiagnosed and treated unnecessarily. Genetic testing can prevent this but is hampered by the challenge of interpreting novel missense variants. Here, we exploit a multiplexed yeast complementation assay to measure both hyper- and hypoactive GCK variation, capturing 97% of all possible missense and nonsense variants. Activity scores correlate with in vitro catalytic efficiency, fasting glucose levels in carriers of GCK variants and with evolutionary conservation. Hypoactive variants are concentrated at buried positions, near the active site, and at a region of known importance for GCK conformational dynamics. Some hyperactive variants shift the conformational equilibrium towards the active state through a relative destabilization of the inactive conformation. Our comprehensive assessment of GCK variant activity promises to facilitate variant interpretation and diagnosis, expand our mechanistic understanding of hyperactive variants, and inform development of therapeutics targeting GCK.