| Literature DB >> 27765496 |
Manuela Antonioli1, Martina Di Rienzo2, Mauro Piacentini2, Gian Maria Fimia3.
Abstract
Autophagy is a major degradative process activated in a rapid and transient manner to cope with stress conditions. Whether autophagy is beneficial or detrimental depends upon the rate of induction and the appropriateness of the duration. Alterations in both autophagy initiation and termination predispose the cell to death, and affect the execution of other inducible processes such as inflammation. In this review we discuss how stress signaling pathways dynamically control the activity of the autophagy machinery by mediating post-translational modifications and regulatory protein interactions. In particular, we highlight the emerging role of TRIM and CULLIN families of ubiquitin ligases which play opposite roles in the autophagy response by promoting or inhibiting, respectively, the activity of the autophagy initiation complex.Entities:
Keywords: AMBRA1; BECLIN-1; CULLIN; Exocyst; IRGM.; TRAF6; TRIM; ULK1
Mesh:
Substances:
Year: 2016 PMID: 27765496 DOI: 10.1016/j.tibs.2016.09.008
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807