FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Mangleburg, C.G., Wu, T., Yalamanchili, H.K., Guo, C., Hsieh, Y.C., Duong, D.M., Dammer, E.B., De Jager, P.L., Seyfried, N.T., Liu, Z., Shulman, J.M. (2020). Integrated analysis of the aging brain transcriptome and proteome in tauopathy.  Mol. Neurodegener. 15(1): 56.
FlyBase ID
FBrf0246868
Publication Type
Research paper
Abstract
Tau neurofibrillary tangle pathology characterizes Alzheimer's disease and other neurodegenerative tauopathies. Brain gene expression profiles can reveal mechanisms; however, few studies have systematically examined both the transcriptome and proteome or differentiated Tau- versus age-dependent changes. Paired, longitudinal RNA-sequencing and mass-spectrometry were performed in a Drosophila model of tauopathy, based on pan-neuronal expression of human wildtype Tau (TauWT) or a mutant form causing frontotemporal dementia (TauR406W). Tau-induced, differentially expressed transcripts and proteins were examined cross-sectionally or using linear regression and adjusting for age. Hierarchical clustering was performed to highlight network perturbations, and we examined overlaps with human brain gene expression profiles in tauopathy. TauWT induced 1514 and 213 differentially expressed transcripts and proteins, respectively. TauR406W had a substantially greater impact, causing changes in 5494 transcripts and 697 proteins. There was a ~ 70% overlap between age- and Tau-induced changes and our analyses reveal pervasive bi-directional interactions. Strikingly, 42% of Tau-induced transcripts were discordant in the proteome, showing opposite direction of change. Tau-responsive gene expression networks strongly implicate innate immune activation. Cross-species analyses pinpoint human brain gene perturbations specifically triggered by Tau pathology and/or aging, and further differentiate between disease amplifying and protective changes. Our results comprise a powerful, cross-species functional genomics resource for tauopathy, revealing Tau-mediated disruption of gene expression, including dynamic, age-dependent interactions between the brain transcriptome and proteome.
PubMed ID
PubMed Central ID
PMC7526226 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Mol. Neurodegener.
    Title
    Molecular Neurodegeneration
    Publication Year
    2006-
    ISBN/ISSN
    1750-1326
    Data From Reference