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FBXW7 coordinates postprandial muscle glucose metabolism and maintenance of skeletal muscle mass

GSE140503 Mus musculus Expression profiling by high throughput sequencing 6 samples Submitted 2024/06/21 Platform GPL21103
Summary
In this study, we show that muscle-specific inactivation of FBXW7 elicits striking defects in postprandial glucose metabolism and failure to maintain skeletal muscle mass in adult mice. Further, mice lacking FBXW7 exhibited impaired endurance capacity and exacerbated HFD-induced insulin resistance and postprandial hyperglycemia. At the mechanistic level, RNAseq and quantitative proteomic analysis revealed global effects of FBXW7 deficiency on skeletal muscle transcriptome and proteome. This work illustrates a prominent role of FBXW7 in integrating postprandial nutritional signals to coordinate glucose metabolism and muscle mass maintenance.
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Also filed as BioProject PRJNA589977 and SRA study SRP230256. Searching any of these in the dataset finder brings you back here.

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