Literature DB >> 35258397

The V-ATPase complex regulates non-canonical Atg8-family protein lipidation through ATG16L1 recruitment.

Lewis Timimi1, Carmen Figueras-Novoa1, Elena Marcassa1, Oliver Florey2, J Kenneth Baillie3, Rupert Beale1,4, Rachel Ulferts1.   

Abstract

Conjugation of the Atg8 (autophagy related 8) family of ubiquitin-like proteins to phospholipids of the phagophore is a hallmark of macroautophagy/autophagy. Consequently, Atg8 family members, especially LC3B, are commonly used as a marker of autophagosomes. However, the Atg8 family of proteins are not found solely attached to double-membrane autophagosomes. In non-canonical Atg8-family protein lipidation they become conjugated to single membranes. We have shown that this process is triggered by recruitment of ATG16L1 by the vacuolar-type H+-translocating ATPase (V-ATPase) proton pump, suggesting a role for pH sensing in recruitment of Atg8-family proteins to single membranes.

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Keywords:  ATG16L1; Atg4; Atg8; CASM; SopF; V-ATPase; influenza; lipidation; non-canonical autophagy

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Year:  2022        PMID: 35258397      PMCID: PMC9037397          DOI: 10.1080/15548627.2022.2029233

Source DB:  PubMed          Journal:  Autophagy        ISSN: 1554-8627            Impact factor:   16.016


  1 in total

1.  Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation.

Authors:  Rachel Ulferts; Elena Marcassa; Lewis Timimi; Liam Changwoo Lee; Andrew Daley; Beatriz Montaner; Suzanne Dawn Turner; Oliver Florey; John Kenneth Baillie; Rupert Beale
Journal:  Cell Rep       Date:  2021-10-26       Impact factor: 9.423

  1 in total

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