Obesity and type 2 diabetes (T2D) are growing health challenges with unmet treatment needs. Traf2- and NCK-interacting protein kinase (TNIK) is a recently identified obesity- and T2D-associated gene with unknown functions. We show that TNIK governs lipid and glucose homeostasis in Drosophila and mice. Loss of the Drosophila ortholog of TNIK, misshapen, altered the metabolite profiles and impaired de novo lipogenesis in high sugar-fed larvae. Tnik knockout mice exhibited hyperlocomotor activity and were protected against diet-induced fat expansion, insulin resistance, and hepatic steatosis. The improved lipid profile of Tnik knockout mice was accompanied by enhanced skeletal muscle and adipose tissue insulin-stimulated glucose uptake and glucose and lipid handling. Using the T2D Knowledge Portal and the UK Biobank, we observed associations of TNIK variants with blood glucose, HbA1c, body mass index, body fat percentage, and feeding behavior. These results define an untapped paradigm of TNIK-controlled glucose and lipid metabolism.
Institut(e)Research Unit Signaling and Translation (SAT)
FörderungenIndependent Research Fund Denmark European Union's Horizon 2020 research and innovation programme, Marie Sklodowska-Curie Finnish Diabetes Research Foundation Novo Nordisk Foundation Maud Kuistila Foundation German Research Foundation, Collaborative Research Center Lundbeck Foundation Academy of Finland Sigrid Juselius Foundation Jane and Aatos Erkko Foundation Hallas-Moller Emerging Investigator Novo Nordisk Foundation Orion Research Foundation