Transcription factor Nrf1 is negatively regulated by its O-GlcNAcylation status

被引:27
|
作者
Chen, Jiayu [1 ,2 ,3 ,4 ]
Liu, Xiping [3 ,4 ]
Lue, Fenglin [1 ,2 ]
Lue, Xinping [4 ]
Ru, Yi [4 ]
Ren, Yonggang [1 ,2 ]
Yao, Libo [4 ]
Zhang, Yiguo [1 ,2 ]
机构
[1] Chongqing Univ, Coll Med Bioengn, Lab Cell Biochem & Gene Regulat, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Fac Life Sci, Chongqing 400044, Peoples R China
[3] Zunyi Med Coll, Dept Biochem & Mol Biol, Zunyi 563000, Peoples R China
[4] Fourth Mil Med Univ, Dept Biochem & Mol Biol, State Key Lab Canc Biol, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Nuclear factor erythroid 2-related factor (Nrf1); O-GlcNAcylation; O-Linked N-acetylglucosamine transferase (OGT); Transcriptional regulation; Post-translational modification; BETA-N-ACETYLGLUCOSAMINIDASE; FACTOR E2-RELATED FACTOR-1; CYTOSOLIC PROTEINS; GLCNAC TRANSFERASE; NUCLEAR; GLYCOSYLATION; GENE; CLONING; EXPRESSION; SURVIVAL;
D O I
10.1016/j.febslet.2015.07.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
O-Linked N-acetylglucosatnine transferase (OGT) was identified as an Nrf1-interacting protein. Herein, we show that Nrf1 enables interaction with OGT and their co-immunoprecipitates are O-GlcNAcylated by the enzyme. The putative O-GlcNAcylation negatively regulates Nrf1/TCF11 to reduce both its protein stability and transactivation activity of target gene expression. The turnover of Nrf1 is enhanced upon overexpression of OGT, which promotes ubiquitination of the CNC-bZIP protein. Furthermore, the serine/theorine-rich sequence of PEST2 degron within Nrf1 is identified to be involved in the protein O-GlcNAcylation by OGT. Overall, Nrf1 is negatively regulated by its O-GlcNAcylation status that depends on the glucose concentrations. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2347 / 2358
页数:12
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