Title :
NFkappaB activation is associated with its O-GlcNAcylation state under hyperglycemic conditions
Abstract :
- The transcription factor NFkappaB is activated by phosphorylation and acetylation and plays important roles in inflammatory and immune responses in the cell
- Additionally, posttranslational modification of the NFkappaB p65 subunit by O-linked N-acetylglucosamine (O-GlcNAc) has been reported, but the modification site of O-GlcNAc on NFkappaB p65 and its exact function have not been elucidated
- In this work, we show that O-GlcNAcylation of NFkappaB p65 decreases binding to IkappaB alpha and increases transcriptional activity under hyperglycemic conditions
- Also, we demonstrate that both Thr-322 and Thr-352 of NFkappaB p65 can be modified with O-GlcNAc, but modification on Thr-352 , not Thr-322 , is important for transcriptional activation
- Our findings suggest that site-specific O-GlcNAcylation may be a reason why NFkappaB activity increases continuously under hyperglycemic conditions
Output (sent_index, trigger,
protein,
sugar,
site):
- 3. p65, , NFkappaB p65, O-GlcNAcylation, -
- 4. modified, , -, O-GlcNAc, Thr-322 and Thr-352
Output(Part-Of) (sent_index,
protein,
site):
- 2. NFkappaB p65, site
- 4. NFkappaB p65, Thr-322 and Thr-352
*Output_Site_Fusion* (sent_index,
protein,
sugar,
site):
- 4. NFkappaB p65, O-GlcNAc, Thr-322 and Thr-352