Abstract

Autophagy is an evolutionarily conserved catabolic process that is essential for maintaining cellular, tissue, and organismal homeostasis. Autophagy-related (ATG) genes are indispensable for autophagosome formation. ATG3 is one of the key genes involved in autophagy, and its homologs are common in eukaryotes. During autophagy, ATG3 acts as an E2 ubiquitin-like conjugating enzyme in the ATG8 conjugation system, contributing to phagophore elongation. ATG3 has also been found to participate in many physiological and pathological processes in an autophagy-dependent manner, such as tumor occurrence and progression, ischemia–reperfusion injury, clearance of pathogens, and maintenance of organelle homeostasis. Intriguingly, a few studies have recently discovered the autophagy-independent functions of ATG3, including cell differentiation and mitosis. Here, we summarize the current knowledge of ATG3 in autophagosome formation, highlight its binding partners and binding sites, review its autophagy-dependent functions, and provide a brief introduction into its autophagy-independent functions.

Highlights

  • Autophagy plays an important role in maintaining cellular energy balance, structural reconstruction, and immunity when cells respond to stress conditions, such as amino acid starvation

  • ATG3 can interact with free ATG12 more preferentially than the ATG12–ATG5 conjugate, and the excess interaction of ATG3 with free ATG12 could partially inhibit the interaction between ATG7 and free ATG12, resulting in the suppression of light chain 3 (LC3) lipidation (Tanida et al, 2002a), likely for the reason that the linear sequence of human ATG3FR that binds to ATG12 and ATG7 is overlapped at the 157–176 amino acids (Qiu et al, 2013; Ohashi and Otomo, 2015)

  • Research has shown that ATG3 is degraded via Tyr203 phosphorylation during etoposide or cisplatin treatment, causing DNA damage in cancer cell lines

Read more

Summary

Introduction

Autophagy plays an important role in maintaining cellular energy balance, structural reconstruction, and immunity when cells respond to stress conditions, such as amino acid starvation. A few autophagy-independent functions of ATG3 were found, indicating that the roles of ATG3 might be more complex.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call