Functional significance of O-linked N-acetylglucosamine protein modification in regulating autophagy

Abstract

Autophagy is a core molecular pathway that preserves cellular and organismal homeostasis. Being susceptible to nutrient availability and stress, eukaryotic cells recycle or degrade internal components via membrane transport pathways to provide sustainable biological molecules and energy sources. The dysregulation of this highly conserved physiological process has been strongly linked to human disease. Post-translational modification, a mechanism that regulates protein function, plays a crucial role in autophagy regulation. O-linked N-acetylglucosamine protein modification (O-GlcNAcylation), a monosaccharide post-translational modification of intracellular proteins, is essential in nutritional and stress regulatory mechanisms. O-GlcNAcylation has emerged as an essential regulatory mechanism of autophagy. It regulates autophagy throughout its lifetime by targeting the core components of the autophagy regulatory network. This review provides an overview of the O-GlcNAcylation of autophagy-associated proteins and their regulation and function in the autophagy pathway. Therefore, this article may contribute to further understanding of the role of O-GlcNAc-regulated autophagy and provide new perspectives for the treatment of human diseases.

Keywords: AMP-activated protein kinase (PubChem SID: 379980424); Autophagy; D-Glucose (PubChem CID: 5793); O-GlcNAc transferase (PubChem CID: 405228932); O-GlcNAcase (PubChem CID: 405229538); O-GlcNAcylation; Post-translational modification; Serine/threonine-protein kinase mTOR (PubChem SID: 472409785); UDP-GlcNAc (PubChem CID:445675).