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Author Notes:

Yafei Cai, ycai@njau.edu.cn

Jinming Huang, hunagjinm@sina.com

QJ: writing original draft and editing. YW: writing-original draft. MX: investigation. JinH: investigation. TZ: Data sorting. XL: Data sorting. FC: review and editing. JinH: editing and supervision and funding acquisition. YC: editing and supervision and funding acquisition. All authors contributed to the article and approved the submitted version.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Subject:

Research Funding:

This work was supported by grants from The National Natural Science Foundation of China (grant number 32270516; 31970413); National Key Research and Development Program of China (grant number 2021YFF1000703); Open Project Program of International Joint Research Laboratory in Universities of Jiangsu Province of China for Domestic Animal Germplasm Resources and Genetic Improvement (grant number IJRLD-KF202205).

Keywords:

  • ER stress
  • UFL1
  • Ufmylation modification
  • genotoxic stress
  • inflammation
  • oncogenic stress
  • Ubiquitin-Protein Ligases
  • Proteins
  • Ubiquitination
  • Ubiquitin

UFL1, a UFMylation E3 ligase, plays a crucial role in multiple cellular stress responses

Tools:

Journal Title:

Frontiers in Endocrinology

Volume:

Volume 14

Publisher:

, Pages 1123124-1123124

Type of Work:

Article | Final Publisher PDF

Abstract:

The UFM1 conjugation system(UFMylation)is a novel type of ubiquitin-like system that plays an indispensable role in maintaining cell homeostasis under various cellular stress. Similar to ubiquitination, UFMylation consists of a three-step enzymatic reaction with E1-like enzymes ubiquitin-like modifier activating enzyme5 (UBA5), E2-like enzymes ubiquitin-fold modifier-conjugating enzyme 1(UFC1), and E3-like ligase UFM1-specific ligase 1 (UFL1). As the only identified E3 ligase, UFL1 is responsible for specific binding and modification of the substrates to mediate numerous hormone signaling pathways and endocrine regulation under different physiological or pathological stress, such as ER stress, genotoxic stress, oncogenic stress, and inflammation. Further elucidation of the UFL1 working mechanism in multiple cellular stress responses is essential for revealing the disease pathogenesis and providing novel potential therapeutic targets. In this short review, we summarize the recent advances in novel UFL1 functions and shed light on the potential challenges ahead, thus hopefully providing a better understanding of UFMylation-mediated cellular stress.

Copyright information:

© 2023 Jiang, Wang, Xiang, Hua, Zhou, Chen, Lv, Huang and Cai

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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