4.3 Article

Promoter Hypermethylation of the Phosphatase DUSP22 Mediates PKA- Dependent TAU Phosphorylation and CREB Activation in Alzheimer's Disease

Journal

HIPPOCAMPUS
Volume 24, Issue 4, Pages 363-368

Publisher

WILEY-BLACKWELL
DOI: 10.1002/hipo.22245

Keywords

epigenetics; DNA methylation; hippocampus; brain and neurodegeneration

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Funding

  1. Cellex Foundation
  2. Botin Foundation
  3. Fundacio Agrupacio Mutua
  4. Health and Science Departments of the Catalan Government (Generalitat de Catalunya)
  5. ICREA Funding Source: Custom

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Genetic screening in Alzheimer's disease (AD) has identified only a handful of genes that are mutated in the disorder. Thus, for a very large proportion of patients, the biology of their disease is poorly understood. Epigenetic alterations may provide an explanation in these cases. Using DNA methylation profiles of human hippocampus from controls and patients, we have identified the presence of promoter hypermethylation of the dual-specificity phosphatase 22 (DUSP22) gene in AD. DUSP22 is a likely candidate gene for involvement in the pathogenesis of the disorder since, as we demonstrate here, it inhibits PKA activity and thereby determines TAU phosphorylation status and CREB signaling. (c) 2014 The Authors. Hippocampus Published by Wiley Periodicals, Inc.

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