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Interaction of neuronal Cdc2-like protein kinase with microtubule-associated protein tau
K Sobue1, A Agarwal-Mawal, W Li
1Bloomfield Center for Research in Aging, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec H3T 1E2, Canada.
Abstract:
Neuronal Cdc2-like protein kinase (NCLK), a approximately 58-kDa heterodimer, was isolated from neuronal microtubules (Ishiguro, K., Takamatsu, M., Tomizawa, K., Omori, A., Takahashi, M., Arioka, M., Uchida, T. and Imahori, K. (1992) J. Biol. Chem. 267, 10897-10901). The biochemical nature of NCLK-microtubule association is not known. In this study we found that NCLK is released from microtubules upon microtubule disassembly as a 450-kDa species. The 450-kDa species is an NCLK.tau complex, and NCLK-bound tau is in a nonphosphorylated state. Tau phosphorylation causes NCLK.tau complex dissociation, and phosphorylated tau does not bind to NCLK. In vitro, the Cdk5 subunit of NCLK binds to the microtubule-binding region of tau and NCLK associates with microtubules only in the presence of tau. Our data indicate that in brain extract NCLK is complexed with tau in a tau phosphorylation-dependent manner and that tau anchors NCLK to microtubules. Recently NCLK has been suggested to be aberrantly activated and to hyperphosphorylate tau in Alzheimer's disease brain (Patrick, G. N., Zukerberg, L., Nikolic, M., de la Monte, S., Dikkes, P, and Tsai, L.-H. (1999) Nature 402, 615-622). Our findings may explain why in Alzheimer's disease NCLK specifically hyperphosphorylates tau, although this kinase has a number of protein substrates in the brain.
Insights
Neuronal Cdc2-like protein kinase (NCLK) binds to tau, anchoring it to microtubules. Tau phosphorylation disrupts this binding, explaining NCLK
Area of Science:
- Neuroscience
- Molecular Biology
- Biochemistry
Background:
- Neuronal Cdc2-like protein kinase (NCLK) is a microtubule-associated protein.
- The mechanism of NCLK's association with microtubules is unknown.
Purpose of the Study:
- To elucidate the biochemical nature of NCLK-microtubule association.
- To investigate the role of tau in NCLK-microtubule binding.
Main Methods:
- Microtubule disassembly and complex isolation.
- In vitro binding assays using NCLK subunits and tau.
- Analysis of tau phosphorylation status.
Main Results:
- NCLK is released from microtubules as a 450-kDa complex with tau.
- NCLK binds to nonphosphorylated tau via its Cdk5 subunit.
- Tau phosphorylation leads to NCLK.tau complex dissociation.
- NCLK associates with microtubules exclusively in the presence of tau.
Conclusions:
- Tau acts as an anchor, mediating NCLK association with microtubules in a phosphorylation-dependent manner.
- These findings provide a potential explanation for NCLK's specific hyperphosphorylation of tau in Alzheimer's disease.