Iwanaga R, Ohtani K, Hayashi T, Nakamura M
Human Gene Sciences Center, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Oncogene. 2001 Apr 19;20(17):2055-67. doi: 10.1038/sj.onc.1204304.
The trans-activator protein Tax of human T-cell leukemia virus type I (HTLV-I) plays an important role in the development of adult T-cell leukemia through, at least in part, its ability to stimulate cell growth. We previously reported that Tax induced cell cycle progression from G0/G1 phase to S and G2/M phases in human T-cell line Kit 225 cells. To elucidate molecular mechanism of Tax-induced cell cycle progression, we systematically examined the effects of Tax on biochemical events associated with cell cycle progression. Introduction of Tax into resting Kit 225 cells induced activation of the G1/S transition regulation cascade consisting of activation of cyclin dependent kinase 2 (CDK2) and CDK4, phosphorylation of the Rb family proteins and an increase in free E2F. The kinase activation was found to result from Tax-induced expression of genes for cell cycle regulatory molecules including cyclin D2, cyclin E, E2F1, CDK2, CDK4 and CDK6, and Tax-induced reduction of CDK inhibitors p19(INK4d) and p27(Kip1). These modulations by Tax always paralleled the ability of Tax to activate the NF-kappaB transcription pathway. These results indicate the important role of Tax-mediated trans-activation of the genes for cell cycle regulatory molecules in Tax-induced cell cycle progression.
人类T细胞白血病病毒I型(HTLV-I)的反式激活蛋白Tax在成人T细胞白血病的发展中起着重要作用,至少部分是通过其刺激细胞生长的能力实现的。我们之前报道过,Tax可诱导人T细胞系Kit 225细胞的细胞周期从G0/G1期进入S期和G2/M期。为阐明Tax诱导细胞周期进程的分子机制,我们系统地研究了Tax对与细胞周期进程相关的生化事件的影响。将Tax导入静止的Kit 225细胞会诱导由细胞周期蛋白依赖性激酶2(CDK2)和CDK4激活、Rb家族蛋白磷酸化以及游离E2F增加所组成的G1/S转换调节级联反应的激活。发现激酶激活是由Tax诱导细胞周期调节分子的基因表达所致,这些分子包括细胞周期蛋白D2、细胞周期蛋白E、E2F1、CDK2、CDK4和CDK6,以及Tax诱导的CDK抑制剂p19(INK4d)和p27(Kip1)的减少。Tax的这些调节作用总是与Tax激活NF-κB转录途径的能力平行。这些结果表明,Tax介导的细胞周期调节分子基因的反式激活在Tax诱导的细胞周期进程中起重要作用。