Interactions between Autophagy Receptors and Ubiquitin-like Proteins Form the Molecular Basis for Selective Autophagy

• Published in: Molecular cell 2014-01, Vol.53 (2), p.167-178
• Main Authors: Rogov, Vladimir, Dötsch, Volker, Johansen, Terje, Kirkin, Vladimir
• Format: Article
• Language: English
• Subjects: Autophagy - physiology; Models, Biological; Models, Molecular; Peroxisomes - metabolism; Signal Transduction; Ubiquitination; Ubiquitins - metabolism; Ubiquitins - physiology
• ISSN: 1097-2765; 1097-4164
• DOI: 10.1016/j.molcel.2013.12.014

Selective autophagy ensures recognition and removal of various cytosolic cargos. Hence, aggregated proteins, damaged organelles, or pathogens are enclosed into the double-membrane vesicle, the autophagosome, and delivered to the lysosome for degradation. This process is mediated by selective autophagy receptors, such as p62/SQSTM1. These proteins recognize autophagic cargo and, via binding to small ubiquitin-like modifiers (UBLs)—Atg8/LC3/GABARAPs and ATG5—mediate formation of selective autophagosomes. Recently, it was found that UBLs can directly engage the autophagosome nucleation machinery. Here, we review recent findings on selective autophagy and propose a model for selective autophagosome formation in close proximity to cargo. Selective autophagy ensures recognition and removal of various cytosolic cargos. In this review article, Rogov et al. highlight recent findings from the literature on selective autophagy and propose a model for selective autophagosome formation in close proximity to cargo.