To further identify the specific type of ubiquitin linkage responsible for NEDD4-mediated YAP1 ubiquitination, we co-transfected HEK293T cells with NEDD4, YAP1, and plasmids encoding various ubiquitin chains, including K6-, K11-, K27-, K29-, K33-, K48-, and K63-linked forms
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This structural change allows for enhanced interaction with IGF-1 receptors, leading to increased activation of the PI3K/Akt pathway, which plays a central role in protein synthesis and cellular regeneration