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Histidine Phosphorylation and Obesity

Project description

Role of histidine phosphorylation in glucose metabolism and obesity

Histidine phosphorylation is crucial for prokaryotic signal transduction and as an intermediate for several metabolic enzymes. Its role is poorly understood as the relative instability of phosphohistidine makes its study difficult. Recent data have implicated histidine phosphorylation dysregulation in heart failure and cancer, and the histidine phosphorylation state has been associated with insulin secretion regulation in the pancreas. The main goal of the EU-funded HisPO project is to determine the role of protein histidine phosphorylation in obesity-associated metabolic dysfunction. Researchers will study global histidine phosphorylation levels in obesity, histidine kinase and phosphatase expression or activity and specific protein histidine phosphorylation. The objective is to evaluate whether a change in histidine phosphorylation levels impacts whole-body glucose metabolism as well as body weight and composition.

Objective

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.

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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

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(opens in new window) H2020-MSCA-IF-2019

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Coordinator

UNIVERSITAT BASEL
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 203 149,44
Address
PETERSPLATZ 1
4051 Basel
Switzerland

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Region
Schweiz/Suisse/Svizzera Nordwestschweiz Basel-Stadt
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 203 149,44
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