TBC1D1 functions as a negative regulator of satellite cells for muscle regeneration.

ABSTRACT: The Rab GTPase activating protein (RabGAP) AS160 translocates from the cytosol into the nucleus acting as a transcriptional co-activator of Signal Transducer and Activator of Transcription 3 (STAT3) to regulate proliferation of muscle satellite cells (MuSCs). How this AS160-STAT3 complex is regulated remains largely unclear yet. Here, we show that TBC1D1, a RabGAP related to AS160, forms a super-complex with AS160 and STAT3 to retain the AS160-STAT3 complex in the cytosol. Phosphorylation of TBC1D1-Thr⁵⁹⁶ by protein kinase B dissociates TBC1D1 from AS160 thus releasing the cytosolic retention of the AS160-STAT3 complex. A non-phosphorylatable alanine substitution of Thr⁵⁹⁶ inhibits MuSC proliferation and impairs repair of injured muscle. In contrast, TBC1D1 deficiency

SUBMITTER: Yang X 

PROVIDER: S-EPMC12627490 | biostudies-literature | 2025 Nov

REPOSITORIES: biostudies-literature