de Falco G, Giordano A
Department of Pathology, Anatomy, and Cell Biology, Sbarro Institute for Cancer Research and Molecular Medicine, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
J Cell Physiol. 1998 Dec;177(4):501-6. doi: 10.1002/(SICI)1097-4652(199812)177:4<501::AID-JCP1>3.0.CO;2-4.
CDK9 is a cdc2-related kinase protein. Previously named PITALRE, this protein is a serine-threonine kinase involved in many physiological processes. Unlike most of the cdc2-like kinases, its activity is not cell cycle-regulated. CDK9 acts preferentially in processes different from cell-cycle regulation, such as differentiation. Its cyclin partners, cyclins of T family, recently have been isolated. CDK9 immunoprecipitates with several unidentified polypeptides that may regulate its kinase activity. CDK9 has been shown to associate with the HIV-Tat protein, suggesting a possible involvement in AIDS. CDK9 recently was shown to be responsible for the kinase activity associated with the TAK complex and with the P-TEFb complex, suggesting activity also in the transcription process.
细胞周期蛋白依赖性激酶9(CDK9)是一种与细胞周期蛋白依赖性激酶2(cdc2)相关的激酶蛋白。该蛋白先前被命名为PITALRE,是一种参与多种生理过程的丝氨酸 - 苏氨酸激酶。与大多数类cdc2激酶不同,其活性不受细胞周期调控。CDK9优先作用于不同于细胞周期调控的过程,如分化。其细胞周期蛋白伴侣,即T家族细胞周期蛋白,最近已被分离出来。CDK9与几种可能调节其激酶活性的未鉴定多肽一起进行免疫沉淀。已证明CDK9与HIV-Tat蛋白相关,提示其可能参与艾滋病。最近发现CDK9负责与TAK复合物和P-TEFb复合物相关的激酶活性,表明其在转录过程中也有活性。