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Updated: May 9, 2026

Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates
Published on: May 10, 2022
FBXW10 is negatively regulated in transcription and expression level by protein O-GlcNAcylation
1State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300071, PR China.
Abstract:
Intricate cross-talks exist among multiple post-translational modifications that play critical roles in various cellular events, such as the control of gene expression and regulation of protein function. Here, the cross-talk between O-GlcNAcylation and ubiquitination was investigated in HEK293T cells. By PCR array, 84 ubiquitination-related genes were explored in transcription level in response to the elevation of total protein O-GlcNAcylation due to over-expression of OGT, inhibition of OGA or GlcN treatment. Varied genes were transcriptionally regulated by using different method. But FBXW10, an F-box protein targeting specific proteins for ubiquitination, could be negatively regulated in all ways, suggesting its regulation by protein O-GlcNAcylation. By RT-PCR and Western blot analysis, it was found that FBXW10 could be sharply down-regulated in mRNA and protein level in GlcN-treated cells in a time-dependent way, in line with the enhancement of protein O-GlcNAcylation. It was also found that endogenous FBXW10 was modified by O-GlcNAc in HEK293T cells, implying O-GlcNAcylation might regulate FBXW10 in multiple levels. These findings indicate that O-GlcNAcylation is involved in the regulation of ubiquitination-related genes, and help us understand the cross-talk between O-GlcNAcylation and ubiquitination.
Insights
This study reveals how O-GlcNAcylation impacts ubiquitination pathways. Elevated O-GlcNAcylation down-regulates FBXW10, an F-box protein, at both mRNA and protein levels, indicating a significant cross-talk.
Area of Science:
- Cellular Biology
- Molecular Biology
- Biochemistry
Background:
- Post-translational modifications (PTMs) are crucial for cellular events.
- Cross-talk between O-GlcNAcylation and ubiquitination is not fully understood.
Purpose of the Study:
- Investigate the cross-talk between O-GlcNAcylation and ubiquitination.
- Identify ubiquitination-related genes regulated by O-GlcNAcylation.
Main Methods:
- PCR array to analyze 84 ubiquitination-related genes.
- RT-PCR and Western blot to assess FBXW10 expression.
- O-GlcNAcylation elevation via OGT overexpression, OGA inhibition, or GlcN treatment in HEK293T cells.
Main Results:
- O-GlcNAcylation elevation transcriptionally regulated various ubiquitination genes.
- FBXW10 (an F-box protein) was consistently down-regulated across different O-GlcNAcylation elevation methods.
- FBXW10 mRNA and protein levels decreased in a time-dependent manner with GlcN treatment.
- Endogenous FBXW10 was found to be modified by O-GlcNAc.
Conclusions:
- O-GlcNAcylation plays a role in regulating ubiquitination-related gene expression.
- O-GlcNAcylation may regulate FBXW10 at multiple levels.
- Findings elucidate the intricate cross-talk between O-GlcNAcylation and ubiquitination pathways.
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