Differential effects of putative N-glycosylation sites in human Tau on Alzheimer's disease-related neurodegeneration

Cell Mol Life Sci. 2021 Mar;78(5):2231-2245. doi: 10.1007/s00018-020-03643-3. Epub 2020 Sep 14.

Abstract

Amyloid assemblies of Tau are associated with Alzheimer's disease (AD). In AD Tau undergoes several abnormal post-translational modifications, including hyperphosphorylation and glycosylation, which impact disease progression. N-glycosylated Tau was reported to be found in AD brain tissues but not in healthy counterparts. This is surprising since Tau is a cytosolic protein whereas N-glycosylation occurs in the ER-Golgi. Previous in vitro studies indicated that N-glycosylation of Tau facilitated its phosphorylation and contributed to maintenance of its Paired Helical Filament structure. However, the specific Tau residue(s) that undergo N-glycosylation and their effect on Tau-engendered pathology are unknown. High-performance liquid chromatography and mass spectrometry (LC-MS) analysis indicated that both N359 and N410 were N-glycosylated in wild-type (WT) human Tau (hTau) expressed in human SH-SY5Y cells. Asparagine to glutamine mutants, which cannot undergo N-glycosylation, at each of three putative N-glycosylation sites in hTau (N167Q, N359Q, and N410Q) were generated and expressed in SH-SY5Y cells and in transgenic Drosophila. The mutants modulated the levels of hTau phosphorylation in a site-dependent manner in both cell and fly models. Additionally, N359Q ameliorated, whereas N410Q exacerbated various aspects of hTau-engendered neurodegeneration in transgenic flies.

Keywords: Drosophila; N-glycosylation; N⟶Q mutation; SH-SY5Y cells; Tau protein.

MeSH terms

  • Alzheimer Disease / genetics*
  • Alzheimer Disease / metabolism
  • Animals
  • Animals, Genetically Modified
  • Binding Sites / genetics
  • Cell Line, Tumor
  • Disease Models, Animal
  • Drosophila / genetics
  • Drosophila / metabolism
  • Glycosylation
  • Humans
  • Longevity / genetics
  • Mutation, Missense*
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / metabolism
  • Phosphorylation
  • tau Proteins / genetics*
  • tau Proteins / metabolism

Substances

  • tau Proteins