Draetta G, Beach D
Cold Spring Harbor Laboratory, New York 11724.
Cell. 1988 Jul 1;54(1):17-26. doi: 10.1016/0092-8674(88)90175-4.
HeLa cell p34, homolog of the yeast cdc2+/CDC28 protein kinase, has been investigated. p34 was phosphorylated at two or more sites and existed in a complex with p13, the previously identified homolog of the suc1+ gene product of S. pombe. A fraction of the most highly phosphorylated form of p34 was also associated with p62, a newly identified protein that became phosphorylated in vitro. The phosphorylation state of p34, its association with p62, and the protein kinase activity of the complex were each subject to cell cycle regulation. In newly born cells early in G1, p34 was unphosphorylated, not associated with p62, and inactive as a protein kinase. Each of these conditions was reversed in G2 and the p34/p62 complex was maximally active as a protein kinase, with respect to both endogenous and exogenous substrates, during mitotic metaphase. p34 may act to regulate the G2/M transition in HeLa cells.
对HeLa细胞中的p34进行了研究,它是酵母cdc2⁺/CDC28蛋白激酶的同源物。p34在两个或更多位点被磷酸化,并与p13形成复合物,p13是先前鉴定的粟酒裂殖酵母suc1⁺基因产物的同源物。p34最高度磷酸化形式的一部分还与p62相关,p62是一种新鉴定的在体外会被磷酸化的蛋白质。p34的磷酸化状态、其与p62的结合以及复合物的蛋白激酶活性均受到细胞周期调控。在G1期早期的新生细胞中,p34未被磷酸化,不与p62结合,且作为蛋白激酶无活性。在G2期,这些情况均发生逆转,并且在有丝分裂中期,p34/p62复合物作为蛋白激酶对内源和外源底物均具有最大活性。p34可能在HeLa细胞中调节G2/M期转换。