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Modulation of synaptic transmission through O-GlcNAcylation.

Seunghyo HanJun-Nyeong KimChan Ho ParkJin-Seok ByunDo-Yeon KimHyoung-Gon Ko
Published in: Molecular brain (2024)
O-GlcNAcylation is a posttranslational modification where N-acetylglucosamine (O-GlcNAc) is attached and detached from a serine/threonine position by two enzymes: O-GlcNAc transferase and O-GlcNAcase. In addition to roles in diabetes and cancer, recent pharmacological and genetic studies have revealed that O-GlcNAcylation is involved in neuronal function, specifically synaptic transmission. Global alteration of the O-GlcNAc level does not affect basal synaptic transmission while the effect on synaptic plasticity is unclear. Although synaptic proteins that are O-GlcNAcylated are gradually being discovered, the mechanism of how O-GlcNAcylated synaptic protein modulate synaptic transmission has only been reported on CREB, synapsin, and GluA2 subunit of AMPAR. Future research enabling the manipulation of O-GlcNAcylation in individual synaptic proteins should reveal hidden aspects of O-GlcNAcylated synaptic proteins as modulators of synaptic transmission.
Keyphrases
  • prefrontal cortex
  • type diabetes
  • cardiovascular disease
  • genome wide
  • metabolic syndrome
  • dna methylation
  • protein kinase
  • young adults
  • blood brain barrier
  • binding protein
  • subarachnoid hemorrhage
  • glycemic control