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

Authors :
Chen, Jiayu
Liu, Xiping
Lü, Fenglin
Liu, Xinping
Ru, Yi
Ren, Yonggang
Yao, Libo
Zhang, Yiguo
Source :
FEBS Letters. Aug2015, Vol. 589 Issue 18, p2347-2358. 12p.
Publication Year :
2015

Abstract

O -Linked N -acetylglucosamine 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00145793
Volume :
589
Issue :
18
Database :
Academic Search Index
Journal :
FEBS Letters
Publication Type :
Academic Journal
Accession number :
108808406
Full Text :
https://doi.org/10.1016/j.febslet.2015.07.030