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CALCOCO2/NDP52 initiates selective autophagy through recruitment of ULK and TBK1 kinase complexes.
Boyle, Keith B; Ravenhill, Benjamin J; Randow, Felix.
Affiliation
  • Boyle KB; a Division of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology , Cambridge , UK.
  • Ravenhill BJ; a Division of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology , Cambridge , UK.
  • Randow F; a Division of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology , Cambridge , UK.
Autophagy ; 15(9): 1655-1656, 2019 09.
Article in En | MEDLINE | ID: mdl-31258038
ABSTRACT
The selective macroautophagy of prospective cargo necessitates activity of the autophagy machinery at cargo-determined locations. Whether phagophore membranes are recruited to, or are generated de novo at, the cargo is unknown. In our recent study we show that damaged Salmonella-containing vacuoles, marked by LGALS8/galectin-8, engage the cargo receptor CALCOCO2/NDP52 to recruit the autophagy-initiating ULK and TBK1 complexes and cause the formation of WIPI2-positive phagophore membranes. CALCOCO2 functions in the induction of autophagy by forming a trimer with RB1CC1/FIP200 and TBKBP1/SINTBAD-AZI2/NAP1, components of the ULK and TBK1 kinase complexes, respectively. Such recruitment of the upstream autophagy machinery to prospective cargo reveals how in complex eukaryotes detection of cargo-associated 'eat me' signals, induction of autophagy, and juxtaposition of cargo and phagophores are integrated.
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Full text: 1 Database: MEDLINE Main subject: Autophagy Type of study: Observational_studies / Risk_factors_studies Language: En Journal: Autophagy Year: 2019 Type: Article Affiliation country: United kingdom

Full text: 1 Database: MEDLINE Main subject: Autophagy Type of study: Observational_studies / Risk_factors_studies Language: En Journal: Autophagy Year: 2019 Type: Article Affiliation country: United kingdom