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A lysosome-to-nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB

    1. [1] Baylor College of Medicine

      Baylor College of Medicine

      Estados Unidos

    2. [2] Columbia University

      Columbia University

      Estados Unidos

    3. [3] University of Texas MD Anderson Cancer Center

      University of Texas MD Anderson Cancer Center

      Estados Unidos

    4. [4] Telethon Institute Of Genetics And Medicine

      Telethon Institute Of Genetics And Medicine

      Nápoles, Italia

    5. [5] BioMarin Pharmaceutical Inc, Novato, CA, USA
    6. [6] Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA, USA; Department of Biology, Massachusetts Institute of Technology (MIT), Cambridge, MA, USA; David H Koch Institute for Integrative Cancer Research at MIT, Cambridge, MA, USA; 0Seven Cambridge Center, Broad Institute, Cambridge, MA, USA; 1Howard Hughes Medical Institute, MIT, Cambridge, MA, USA
    7. [7] Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA, USA; Department of Biology, Massachusetts Institute of Technology (MIT), Cambridge, MA, USA; David H Koch Institute for Integrative Cancer Research at MIT, Cambridge, MA, USA
  • Localización: EMBO journal: European Molecular Biology Organization, ISSN 0261-4189, Vol. 31, Nº. 5, 2012, págs. 1095-1108
  • Idioma: inglés
  • Enlaces
  • Resumen
    • Under basal conditions TFEB, a master regulator of lysosomal biogenesis, is sequestered in the cytosol due to mTORC1-dependent phosphorylation at the lysosomal membrane. Nutrient starvation or lysosomal dysfunction inhibit mTORC1 activity and induce nuclear translocation of TFEB inducing target gene expression.


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