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The ULK complex initiates autophagosome formation at phosphatidylinositol synthase-enriched ER subdomains.

Taki NishimuraNoboru Mizushima
Published in: Autophagy (2017)
In our recent paper, we biochemically analyzed autophagosome-related membranes at the initiation stage of macroautophagy/autophagy using atg knockout (KO) cells and demonstrated that the ULK complex is recruited to 2 distinct membranes: the ER membrane and ATG9A-positive autophagosome precursors. We have also identified phosphatidylinositol synthase (PIS)-enriched ER subdomains as the initiation site of autophagosome formation. Based on these findings, we propose that the ULK complex, the PIS-enriched ER subdomain, and ATG9A vesicles together initiate autophagosome formation.
Keyphrases
  • endoplasmic reticulum
  • estrogen receptor
  • breast cancer cells
  • oxidative stress
  • signaling pathway
  • cell cycle arrest
  • protein kinase