mTOR activates the VPS34–UVRAG complex to regulate autolysosomal tubulation and cell survival

• Michael J Munson ^[2] ; George FG Allen ^[2] ; Rachel Toth ^[2] ; David G Campbell ^[2] ; John M Lucocq ^[1] ; Ian G Ganley ^[2]
  1. [1] University of St Andrews

     University of St Andrews

     Reino Unido

     
  2. [2] 1 MRC Protein Phosphorylation and Ubiquitylation Unit, College of Life Sciences, University of Dundee Dundee, UK
• Localización: EMBO journal: European Molecular Biology Organization, ISSN 0261-4189, Vol. 34, Nº. 17, 2015, págs. 2272-2290
• Idioma: inglés
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• Resumen

  • Lysosomes are essential organelles that function to degrade and recycle unwanted, damaged and toxic biological components. Lysosomes also act as signalling platforms in activating the nutrient-sensing kinase mTOR. mTOR regulates cellular growth, but it also helps to maintain lysosome identity by initiating lysosomal tubulation through a process termed autophagosome-lysosome reformation (ALR). Here we identify a lysosomal pool of phosphatidylinositol 3-phosphate that, when depleted by specific inhibition of the class III phosphoinositide 3-kinase VPS34, results in prolonged lysosomal tubulation. This tubulation requires mTOR activity, and we identified two direct mTOR phosphorylation sites on UVRAG (S550 and S571) that activate VPS34. Loss of these phosphorylation sites reduced VPS34 lipid kinase activity and resulted in an increase in number and length of lysosomal tubules. In cells in which phosphorylation at these UVRAG sites is disrupted, the result of impaired lysosomal tubulation alongside ALR activation is massive cell death. Our data imply that ALR is critical for cell survival under nutrient stress and that VPS34 is an essential regulatory element in this process.