Affiliation:
1. Department of Life Science, Laboratory of Functional Glycomics, Ajou University, San 5, Wonchon-dong, Suwon 443-
749, Korea
Abstract
Introduction:
Protein S-nitrosylation (SNO) and O-GlcNAcylation are important
posttranslational modifications. The biological connection between SNO and O-GlcNAcylation is
not clear.
Objective:
We aim to identify the crosstalk between SNO and O-GlcNAcylation during heat-shock.
Methods:
Ex vivo heat-shock on mouse tissues together with in vitro heat-shock on culture cells was
performed and global levels of SNO and O-GlcNAcylation were analyzed with Biotin-switch assay
(BSA) and RL2 immunoblots.
Results:
Heat-shock induces hypo-SNO in parallel with hyper-O-GlcNAcylation. Inverted induction
of hypo-SNO and hyper-O-GlcNAcylation is globally progressed in a time-dependent manner.
Discussion:
Moreover, heat-shock ubiquitously facilitates S-denitrosylation (SdeNO) of
endogenous SNO-proteins including SNO-OGT, SNO-Hsp70, SNO-Hsp90, SNO-Akt, and SNOactin.
Particularly, SdeNO of SNO-OGT leads to enhanced OGT activity.
Conclusion:
These findings provide mechanistic evidence that heat-shock triggers SdeNO of SNOOGT
by which OGT activity is up-regulated, resulting in hyper-O-GlcNAcylation.
Funder
Intramural Ajou Research, Korea Grants
Publisher
Bentham Science Publishers Ltd.
Subject
Biochemistry,General Medicine,Structural Biology
Cited by
1 articles.
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