| Autor: |
Jitendra S. Kanshana, Erin E. Kershaw, Samantha L. Rosenthal, Nicola L. Hawley, Dan E Weeks, Ashlee N Wood, Aneta Kowalski, Ray Lu, Sebastien Gingras, Brett A. Kaufman, Gabriele Schoiswohl, Polly E. Mattila, Stephen T. McGarvey, Michael Ewing, Anna C. Meyer, Ryan L. Minster |
| Rok vydání: |
2021 |
| Předmět: |
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| Popis: |
Obesity and diabetes have strong heritable components, yet the genetic contributions to these diseases remain largely unexplained. In humans, a missense variant in Creb3 regulatory factor (CREBRF) [rs373863828 (p.Arg457Gln); CREBRFR457Q] is strongly associated with increased odds of obesity but decreased odds of diabetes. Although virtually nothing is known about CREBRF’s mechanism of action, emerging evidence implicates it in the adaptive transcriptional response to nutritional stress downstream of TORC1. The objectives of this study were to generate a murine model with knockin of the orthologous variant in mice (CREBRFR458Q) and to test the hypothesis that this CREBRF variant promotes obesity and protects against diabetes by regulating energy and glucose homeostasis downstream of TORC1. To test this hypothesis, we performed extensive phenotypic analysis of CREBRFR458Q knockin mice at baseline and in response to acute (fasting/refeeding), chronic (low- and high-fat diet feeding), and extreme (prolonged fasting) nutritional stress as well as with pharmacological TORC1 inhibition. The results demonstrate that the murine CREBRFR458Q model of the human CREBRFR457Q variant does not influence energy/glucose homeostasis in response to these interventions. Alternative preclinical models and/or studies in humans will be required to decipher the mechanisms linking this variant to human health and disease. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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