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TAK1 activation of alpha-TAT1 and microtubule hyperacetylation control AKT signaling and cell growth.

Nirav Shah | Sanjay Kumar | Naveed Zaman | Christopher C Pan | Jeffrey C Bloodworth | Wei Lei | John M Streicher | Nadine Hempel | Karthikeyan Mythreye | Nam Y Lee
Nature communications | 2018

Acetylation of microtubules (MT) confers mechanical stability necessary for numerous functions including cell cycle and intracellular transport. Although αTAT1 is a major MT acetyltransferase, how this enzyme is regulated remains much less clear. Here we report TGF-β-activated kinase 1 (TAK1) as a key activator of αTAT1. TAK1 directly interacts with and phosphorylates αTAT1 at Ser237 to critically enhance its catalytic activity, as mutating this site to alanine abrogates, whereas a phosphomimetic induces MT hyperacetylation across cell types. Using a custom phospho-αTAT1-Ser237 antibody, we screen various mouse tissues to discover that brain contains some of the highest TAK1-dependent αTAT1 activity, which, accordingly, is diminished rapidly upon intra-cerebral injection of a TAK1 inhibitor. Lastly, we show that TAK1 selectively inhibits AKT to suppress mitogenic and metabolism-related pathways through MT-based mechanisms in culture and in vivo. Collectively, our findings support a fundamental new role for TGF-β signaling in MT-related functions and disease.

Pubmed ID: 29703898

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01 CA178443

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