4.5 Article

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

Journal

FEBS LETTERS
Volume 589, Issue 18, Pages 2347-2358

Publisher

WILEY
DOI: 10.1016/j.febslet.2015.07.030

Keywords

Nuclear factor erythroid 2-related factor (Nrf1); O-GlcNAcylation; O-Linked N-acetylglucosamine transferase (OGT); Transcriptional regulation; Post-translational modification

Funding

  1. National Natural Science Foundation of China (NSFC) [91129703, 91429305, 31270879]
  2. NSFC [31270879, 31470803]
  3. State Key Laboratory of Cancer Biology at Fourth Military Medical University [CBSKL201312, CBSK201203]

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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.

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