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HisPO - Histidine Phosphorylation and Obesity
Third-party funded project
Project title HisPO - Histidine Phosphorylation and Obesity
Principal Investigator(s) Hall, Michael N.
Co-Investigator(s) Thomas, Amandine
Organisation / Research unit Departement Biozentrum / Biochemistry (Hall)
Project start 01.05.2020
Probable end 30.04.2022
Status Completed
Abstract

Histidine PhosPhorylation and Obesity Protein histidine phosphorylation is a poorly characterized post-translational modification. Its importance in mammalian cellular function is emerging from the discovery of histidine kinases and phosphatases and their substrates. Recently, histidine phosphorylation has been involved in heart failure and cancer. Obesity and type 2 diabetes remain challenging disorders due to growing prevalence around the world and poorly efficient treatments. Regarding metabolic disorders, histidine phosphorylation state has been associated with insulin secretion regulation in pancreas. However, the role of histidine phosphorylation in insulin sensitivity in liver, skeletal muscle or adipose tissue and/or in obesity is still not known. The main aim of the present project is to determine whether protein histidine phosphorylation plays a role in obesity-associated metabolic dysfunction. Thus, we will determine if obesity modify global histidine phosphorylation level, histidine kinases and phosphatases expression or activity, and specific protein histidine phosphorylation. Then, we will evaluate whether a change of histidine phosphorylation level can impact whole-body glucose metabolism and body weight/composition by using transgenic mice deficient in histidine phosphatases and/or kinases.

Keywords Obesity, insulin resistance, diabetes, histidine phosphorylation
Financed by Commission of the European Union
   

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20/04/2024