Meyerson M, Enders G H, Wu C L, Su L K, Gorka C, Nelson C, Harlow E, Tsai L H
Massachusetts General Hospital Cancer Center, Charlestown 02129.
EMBO J. 1992 Aug;11(8):2909-17. doi: 10.1002/j.1460-2075.1992.tb05360.x.
The p34cdc2 protein kinase is known to regulate important transitions in the eukaryotic cell cycle. We have identified 10 human protein kinases based on their structural relation to p34cdc2. Seven of these kinases are novel and the products of five share greater than 50% amino acid sequence identity with p34cdc2. The seven novel genes are broadly expressed in human cell lines and tissues with each displaying some cell type or tissue specificity. The cdk3 gene, like cdc2 and cdk2, can complement cdc28 mutants of Saccharomyces cerevisiae, suggesting that all three of these protein kinases can play roles in the regulation of the mammalian cell cycle. The identification of a large family of cdc2-related kinases opens the possibility of combinatorial regulation of the cell cycle together with the emerging large family of cyclins.
已知p34cdc2蛋白激酶可调节真核细胞周期中的重要转变。我们基于与p34cdc2的结构关系鉴定出了10种人类蛋白激酶。其中7种激酶是新发现的,且5种激酶的产物与p34cdc2的氨基酸序列同一性超过50%。这7个新基因在人类细胞系和组织中广泛表达,每个基因都表现出一定的细胞类型或组织特异性。cdk3基因与cdc2和cdk2一样,能够互补酿酒酵母的cdc28突变体,这表明这三种蛋白激酶都可能在哺乳动物细胞周期的调节中发挥作用。一大类与cdc2相关的激酶的鉴定,为与新出现的一大类细胞周期蛋白一起对细胞周期进行组合调节开辟了可能性。