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2000
Volume 6, Issue 5
  • ISSN: 1567-2050
  • E-ISSN: 1875-5828

Abstract

The aggregation of the microtubule-associated protein tau into paired-helical filaments is the defining characteristic of the tauopathies. It has become apparent that the hyperphosphorylation of tau likely plays a role in the aggregation process and thus strategies to reduce tau phosphorylation are generating wide interest. The O-GlcNAc posttranslational modification of tau has been shown to be reciprocal to its phosphorylation; increasing O-GlcNAc leads to reductions in tau phosphorylation. In this mini-review, we highlight the use of chemical compounds as a means of understanding the reciprocal nature of tau phosphorylation and tau O-GlcNAcylation and highlight some recent progress in this area.

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/content/journals/car/10.2174/156720509789207967
2009-10-01
2025-08-14
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/content/journals/car/10.2174/156720509789207967
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  • Article Type:
    Research Article
Keyword(s): glucosaminidase; glycoside hydrolase; O-GlcNAc; phosphorylation; Tau
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