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Cyclin-dependent protein kinase 5 primes microtubule-associated protein tau site-specifically for glycogen synthase kinase 3 beta

机译:细胞周期蛋白依赖性蛋白激酶5引发微管相关蛋白tau位点特异性糖原合酶激酶3 beta

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摘要

In the preceding paper, we showed that GSK3 beta phosphorylates tau at S-202, T-321, S-396, and S-400 in vivo. Phosphorylation of S-202 occurs without priming. Phosphorylation of T-231, on the other hand, requires priming phosphorylation of S-235. Similarly, priming phosphorylation of S-404 is essential for the sequential phosphorylation of S-400 and S-396 by GSK3 beta. The priming kinase that phosphorylates tau at S-235 and S-404 in the brain is not known. In this study, we find that in HEK-293 cells cotransfected with tau, GSK3 beta, and Cdk5, Cdk5 phosphorylates tau at S-202, S-235, and S-404. S-235 phosphorylation enhances GSK3 beta-catalyzed T-231 phosphorylation. Similarly, Cdk5 by phosphorylating S-404 stimulates phosphorylation of S-400 and S-396 by GSK3 beta. These data indicate that Cdk5 primes tau for GSK3 beta in intact cells. To evaluate if Cdk5 primes tau for GSK3 beta in mammalian brain, we examined localizations of Cdk5, tau, and GSK3 beta in rat brain. We also analyzed the interaction of Cdk5 with tau and GSK3 beta in brain microtubules. We found that Cdk5, GSK3 beta, and tau are virtually colocalized in rat brain cortex. When bovine brain microtubules are analyzed by FPLC gel filtration, Cdk5, GSK3 beta, and tau coelute within an similar to 450 kDa complex. From the fractions containing the similar to 450 kDa complex, tau, Cdk5, and GSK3 beta co-immunoprecipitate with each other. In HEK-293 cells transfected with tau, Cdk5, and GSK3 beta in different combinations, tau binds to Cdk5 in a manner independent of GSK3 beta and to GSK3 beta in a manner independent of Cdk5. However, Cdk5 and GSK3 beta bind to each other only in the presence of tau, suggesting that tau connects Cdk5 and GSK3 beta. Our results suggest that in the brain, tau, Cdk5, and GSK3 beta are components of an similar to 450 kDa complex. Within the complex, Cdk5 phosphorylates tau at S-235 and primes it for phosphorylation of T-231 by GSK3 beta. Similarly, Cdk5 by phosphorylating tau at S-404 primes tau for a sequential phosphorylation of S-400 and S-396 by GSK3 beta.
机译:在之前的论文中,我们显示了GSK3β在体内会在S-202,T-321,S-396和S-400处磷酸化tau。 S-202的磷酸化没有引发。另一方面,T-231的磷酸化需要引发S-235的磷酸化。同样,S-404的引发磷酸化对于GSK3 beta对S-400和S-396的顺序磷酸化至关重要。使大脑中S-235和S-404的tau磷酸化的启动激酶尚不清楚。在这项研究中,我们发现在与tau,GSK3 beta和Cdk5共转染的HEK-293细胞中,Cdk5磷酸化了S-202,S-235和S-404的tau。 S-235磷酸化增强了GSK3β催化的T-231磷酸化。同样,Cdk5通过使S-404磷酸化,可以刺激GSK3 beta激活S-400和S-396的磷酸化。这些数据表明,Cdk5启动了完整细胞中GSK3 beta的tau蛋白。为了评估Cdk5是否在哺乳动物脑中为GSK3 beta启动了tau蛋白,我们研究了大鼠脑中Cdk5,tau和GSK3 beta的定位。我们还分析了脑微管中Cdk5与tau和GSK3 beta的相互作用。我们发现Cdk5,GSK3 beta和tau实际上在大鼠大脑皮层中共定位。通过FPLC凝胶过滤分析牛脑微管时,Cdk5,GSK3 beta和tau洗脱液的浓度约为450 kDa。从含有相似的450 kDa复合物的馏分中,tau,Cdk5和GSK3β相互免疫沉淀。在以不同组合转染了tau,Cdk5和GSK3 beta的HEK-293细胞中,tau以独立于GSK3 beta的方式与Cdk5结合,并以独立于Cdk5的方式与GSK3 beta结合。但是,Cdk5和GSK3 beta仅在存在tau的情况下彼此结合,这表明tau连接Cdk5和GSK3 beta。我们的结果表明,在大脑中,tau,Cdk5和GSK3 beta是与450 kDa复合物相似的成分。在复合物中,Cdk5使t-S-235处的tau磷酸化,并引发其被GSK3 beta磷酸化T-231。类似地,Cdk5通过在S-404处将tau磷酸化而引发tau,从而被GSK3 beta依次磷酸化S-400和S-396。

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