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p35是细胞周期蛋白依赖性激酶5的一种神经特异性调节亚基。

p35 is a neural-specific regulatory subunit of cyclin-dependent kinase 5.

作者信息

Tsai L H, Delalle I, Caviness V S, Chae T, Harlow E

机构信息

Massachusetts General Hospital Cancer Center, Charlestown 02129.

出版信息

Nature. 1994 Sep 29;371(6496):419-23. doi: 10.1038/371419a0.

Abstract

Cyclin-dependent kinase 5 (Cdk5) was originally isolated through its structural homology to human Cdc2, a key regulator of cell-cycle progression. In tissue samples from adult mice, Cdk5 protein is found at the highest level in brain, at an intermediate level in testis, and at low or undetectable levels in all other tissues, but brain is the only tissue that shows Cdk5 histone H1 kinase activity. No equivalent kinase activity has been found in tissue culture cell lines despite high levels of Cdk5. This raised the possibility that a Cdk5 regulatory subunit was responsible for the activation of Cdk5 in brain. Here we describe the cloning and characterization of a regulatory subunit for Cdk5 known as p35. p35 displays a neuronal cell-specific pattern of expression, it associates physically with Cdk5 in vivo and activates the Cdk5 kinase. p35 differs from the mammalian cyclins and thus represents a new type of regulatory subunit for cyclin-dependent kinase activity.

摘要

细胞周期蛋白依赖性激酶5(Cdk5)最初是通过其与人类Cdc2(细胞周期进程的关键调节因子)的结构同源性而分离出来的。在成年小鼠的组织样本中,Cdk5蛋白在脑中含量最高,在睾丸中含量中等,而在所有其他组织中含量低或检测不到,但脑是唯一显示Cdk5组蛋白H1激酶活性的组织。尽管组织培养细胞系中Cdk5水平很高,但未发现等效的激酶活性。这就提出了一种可能性,即Cdk5调节亚基负责脑中Cdk5的激活。在这里,我们描述了一种名为p35的Cdk5调节亚基的克隆和特性。p35表现出神经元细胞特异性的表达模式,它在体内与Cdk5物理结合并激活Cdk5激酶。p35不同于哺乳动物的细胞周期蛋白,因此代表了一种新型的细胞周期蛋白依赖性激酶活性调节亚基。

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