1. Academic Validation
  2. O-GlcNAcylation orchestrates porcine oocyte maturation through maintaining mitochondrial dynamics and function

O-GlcNAcylation orchestrates porcine oocyte maturation through maintaining mitochondrial dynamics and function

  • Mol Hum Reprod. 2024 Jan 23:gaae003. doi: 10.1093/molehr/gaae003.
Wen-Jie Xiong 1 Xin-Le Lai 1 Jie Lu 2 Li-Shu Li 1 Jin-Xin Zhang 1 Xing Duan 1
Affiliations

Affiliations

  • 1 Key Laboratory of Applied Technology on Green-Eco-Healthy Animal Husbandry of Zhejiang Province, College of Animal Science and Technology & College of Veterinary Medicine, Zhejiang A&F University, Hangzhou, 311300, China.
  • 2 Department of Cardiovascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai, 200433, China.
Abstract

O-GlcNAc modification exists widely in cells, and the signaling pathways involved in the regulation of important biological processes such as transcription, translation, metabolism and cell cycle. O-GlcNAc modification is an inducible reversible dynamic protein post-translational modification, which regulates complex cellular activities through transient glycosylation and deglycosylation. O-GlcNAc glycosylation is specifically regulated by O-GlcNAc glycosyltransferase (O-GlcNAc transferase, OGT) and O-GlcNAc glycoside hydrolase (O-GlcNAcase, OGA). However, the mechanisms underlying the effects of O-GlcNAc modification on the female reproductive system, especially oocyte quality, remain unclear. Here, we found that after OGT was inhibited, porcine oocytes failed to extrude the first polar body and exhibited abnormal actin and microtubule assembly. Meanwhile, the mitochondrial dynamics and function were also disrupted after inhibition of OGT function, resulting in the occurrence of oxidative stress and Autophagy. Collectively, these results inform our understanding of the importance of the glycosylation process for oocytes maturation, especially for the maturation quality of porcine oocytes, and the alteration of O-GlcNAc in oocytes to regulate cellular events deserves further investigation.

Keywords

O-GlcNAc modification; autophagy; oocyte/mitochondria; oxidative stress.

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