Wherefore Art Tau? Functional importance of site-specific tau phosphorylation in diverse subcellular domains

• Published in: The international journal of biochemistry & cell biology 2023-11, Vol.164, p.106475, Article 106475
• Main Authors: Schneeweis, Amanda, Pak, Daniel T.S.
• Format: Article
• Language: English
• Subjects: Axon; Dendrite; Dendritic spine; Microtubules - metabolism; Neurons - metabolism; Phosphorylation; Synapse; Tau; Tau phosphorylation; tau Proteins - metabolism
• ISSN: 1357-2725; 1878-5875; 1878-5875
• DOI: 10.1016/j.biocel.2023.106475

Tau has canonically been considered as an axonal protein, but studies have observed tau localization in other subcellular domains of neurons. This relocated tau has been identified in both physiological and pathological conditions, and it is often labeled mislocalized. Furthermore, these forms of tau are referred to as “hyperphosphorylated” without specifying the phosphosites involved. On the contrary, we speculate that tau may have multiple physiological functions in various locations regulated via specific phosphorylation sites, although this picture is obscured by a lack of comprehensive phosphosite analysis. Here, we examine findings in the literature on the subcellular location of tau and potential roles tau has in those regions. We intentionally focus on the site-specific phosphorylated patterns involved in governing these properties, which are not well elucidated. To facilitate understanding of these events, we have begun establishing a comprehensive map of tau phosphorylation signatures. Such efforts may clarify tau’s diverse physiological functions beyond the axon as well as promote development of novel therapeutic strategies directed against distinct tau subpopulations.