MAP4K3 mediates amino acid-dependent regulation of autophagy via phosphorylation of TFEB.

Journal Article (Journal Article)

Autophagy is the major cellular pathway by which macromolecules are degraded, and amino acid depletion powerfully activates autophagy. MAP4K3, or germinal-center kinase-like kinase, is required for robust cell growth in response to amino acids, but the basis for MAP4K3 regulation of cellular metabolic disposition remains unknown. Here we identify MAP4K3 as an amino acid-dependent regulator of autophagy through its phosphorylation of transcription factor EB (TFEB), a transcriptional activator of autophagy, and through amino acid starvation-dependent lysosomal localization of MAP4K3. We document that MAP4K3 physically interacts with TFEB and MAP4K3 inhibition is sufficient for TFEB nuclear localization, target gene transactivation, and autophagy, even when mTORC1 is activated. Moreover, MAP4K3 serine 3 phosphorylation of TFEB is required for TFEB interaction with mTORC1-Rag GTPase-Ragulator complex and TFEB cytosolic sequestration. Our results uncover a role for MAP4K3 in the control of autophagy and reveal MAP4K3 as a central node in nutrient-sensing regulation.

Full Text

Duke Authors

Cited Authors

  • Hsu, CL; Lee, EX; Gordon, KL; Paz, EA; Shen, W-C; Ohnishi, K; Meisenhelder, J; Hunter, T; La Spada, AR

Published Date

  • March 5, 2018

Published In

Volume / Issue

  • 9 / 1

Start / End Page

  • 942 -

PubMed ID

  • 29507340

Pubmed Central ID

  • PMC5838220

Electronic International Standard Serial Number (EISSN)

  • 2041-1723

Digital Object Identifier (DOI)

  • 10.1038/s41467-018-03340-7


  • eng

Conference Location

  • England