PUBLICATION

Gender-Specific Expression of Ubiquitin-Specific Peptidase 9 Modulates Tau Expression and Phosphorylation: Possible Implications for Tauopathies

Authors
Köglsberger, S., Cordero-Maldonado, M.L., Antony, P., Forster, J.I., Garcia, P., Buttini, M., Crawford, A., Glaab, E.
ID
ZDB-PUB-161124-12
Date
2017
Source
Molecular neurobiology   54(10): 7979-7993 (Journal)
Registered Authors
Cordero-Maldonado, Maria Lorena, Crawford, Alexander
Keywords
Alzheimer’s disease, Gender differences, Tau, Tauopathies, Transcriptomics, Zebrafish
MeSH Terms
  • Alzheimer Disease/metabolism*
  • Animals
  • Brain/metabolism
  • Female
  • Gene Expression Regulation, Developmental/physiology*
  • Humans
  • Male
  • Phosphorylation
  • Tauopathies/metabolism*
  • Ubiquitin-Specific Proteases/metabolism*
  • Zebrafish
  • tau Proteins/metabolism*
PubMed
27878758 Full text @ Mol. Neurobiol.
Abstract
Public transcriptomic studies have shown that several genes display pronounced gender differences in their expression in the human brain, which may influence the manifestations and risk for neuronal disorders. Here, we apply a transcriptome-wide analysis to discover genes with gender-specific expression and significant alterations in public postmortem brain tissue from Alzheimer's disease (AD) patients compared to controls. We identify the sex-linked ubiquitin-specific peptidase 9 (USP9) as an outstanding candidate gene with highly significant expression differences between the genders and male-specific underexpression in AD. Since previous studies have shown that USP9 can modulate the phosphorylation of the AD-associated protein MAPT, we investigate functional associations between USP9 and MAPT in further detail. After observing a high positive correlation between the expression of USP9 and MAPT in the public transcriptomics data, we show that USP9 knockdown results in significantly decreased MAPT expression in a DU145 cell culture model and a concentration-dependent decrease for the MAPT orthologs mapta and maptb in a zebrafish model. From the analysis of microarray and qRT-PCR experiments for the knockdown in DU145 cells and prior knowledge from the literature, we derive a data-congruent model for a USP9-dependent regulatory mechanism modulating MAPT expression via BACH1 and SMAD4. Overall, the analyses suggest USP9 may contribute to molecular gender differences observed in tauopathies and provide a new target for intervention strategies to modulate MAPT expression.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping