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人类葡萄糖激酶变构活性的综合图谱。

A comprehensive map of human glucokinase variant activity.

机构信息

The Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen, Denmark.

Donnelly Centre, University of Toronto, Toronto, ON, M5S 3E1, Canada.

出版信息

Genome Biol. 2023 Apr 26;24(1):97. doi: 10.1186/s13059-023-02935-8.

Abstract

BACKGROUND

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.

RESULT

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.

CONCLUSION

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.

摘要

背景

葡萄糖激酶(GCK)调节胰岛素分泌以维持适当的血糖水平。序列变异可以改变 GCK 的活性,导致高胰岛素血症性低血糖或与年轻的葡萄糖激酶-成人发病型糖尿病(GCK-MODY)相关的高血糖,这些共同影响了全球多达 1000 万人。GCK-MODY 患者经常被误诊和不必要地治疗。基因测试可以预防这种情况,但受到解释新错义变异的挑战的阻碍。

结果

在这里,我们利用一种多重酵母互补测定法来测量高活性和低活性的 GCK 变异,从而捕获了所有可能的错义和无义变异的 97%。活性评分与体外催化效率、携带 GCK 变异的个体的空腹血糖水平以及进化保守性相关。低活性变异集中在埋藏位置,靠近活性部位,以及已知对 GCK 构象动力学重要的区域。一些高活性变异通过相对不稳定无活性构象,将构象平衡向活性状态转移。

结论

我们对 GCK 变异活性的全面评估有望促进变异解释和诊断,扩展我们对高活性变异的机制理解,并为靶向 GCK 的治疗药物的开发提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ed/10131484/ab27c608b404/13059_2023_2935_Fig1_HTML.jpg

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