Autophagy is a process by which eukaryotic cells degrade and recycle proteins and organelles using intracellular lysosomes. Malfunctions in autophagy have been shown to induce many diseases including cancer, neurodegeneration, diabetes, autoimmunity, and cardiovascular diseases.
Autophagy and Ubiquitin
Autophagy can be induced by many intra- and extra-cellular stress conditions such as endoplasmic reticulum stress, oxidative stress, starvation, growth factor depletion, and osmotic stress. It starts with the formation of double-membrane autophagosomes, which engulf all the cargos of cytoplasm. The autophagosomes fuse with the lysosomes and release the cargos to the highly acidic and hydrolytic environment, which leads to the degradation and recycling of the cellular building blocks across the lysosomal membrane. There are two major types of autophagy- (1) non-selective autophagy (bulk autophagy); and (2) selective autophagy. Selective autophagy is regulated by the ubiquitylation on the aggregated cargo proteins.
Ubiquitylation plays a critical role in selective autophagy. Attachment of ubiquitin molecule to normally long-lived cytoplasmic proteins or to organelles has been shown to result in p62-dependent autophagic degradation. p62 as well as Nbr1, both contain an ubiquitin-binding domain at their extreme C-termini, work as cargo adaptors that allow the recognition of K48- or K63-linked polyubiquitylated proteins.