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I型人类T细胞白血病病毒癌基因产物Tax诱导的细胞类型特异性E2F激活和细胞周期进程

Cell type-specific E2F activation and cell cycle progression induced by the oncogene product Tax of human T-cell leukemia virus type I.

作者信息

Ohtani K, Iwanaga R, Arai M, Huang Y, Matsumura Y, Nakamura M

机构信息

Human Gene Sciences Center, School of Medicine, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.

出版信息

J Biol Chem. 2000 Apr 14;275(15):11154-63. doi: 10.1074/jbc.275.15.11154.

Abstract

The transactivator protein Tax of human T-cell leukemia virus type I plays an important role in the development of adult T-cell leukemia probably through modulation of growth regulatory molecules including p16(INK4a). The molecular mechanism of leukemogenesis induced by Tax has yet to be elucidated. We analyzed Tax function in the cell cycle using an interleukin-2 (IL-2)-dependent human T-cell line (Kit 225) that can undergo cell cycle arrest at G(0)/G(1) phase by deprivation of IL-2. Tax activated endogenous E2F activity in IL-2-starved Kit 225 cells, resulting in activation of E2F site-carrying promoters of genes involved in G(1) to S phase transition in a cell type-dependent and p16(INK4a)-independent manner. The ability of Tax mutants to activate E2F coincided with that to activate nuclear factors kappaB and AT, sole expression of which, however, did not activate E2F, suggesting involvement of another pathway in activation of E2F. Introduction of Tax by a recombinant adenovirus induced cell cycle progression to G(2)/M phase in resting Kit 225 cells accompanied by endogenous cyclin D2 gene expression. Similarly, Tax-induced cell cycle progression was seen with peripheral blood lymphocytes prestimulated with phytohemagglutinin. Analyses with Tax mutants did not allow Tax-induced cell cycle progression to be differentiated from Tax-dependent activation of E2F, suggesting that Tax induces cell cycle progression presumably through activation of E2F. Nevertheless, infection with an E2F1-expressing virus, which is sufficient for induction of S phase in serum-starved fibroblasts, was not sufficient for either E2F activation or cell cycle progression in IL-2-starved Kit 225 cells, implying differential regulation of E2F activation and cell cycle progression in T-cells that is activated by Tax.

摘要

I型人类T细胞白血病病毒的反式激活蛋白Tax可能通过调节包括p16(INK4a)在内的生长调节分子,在成人T细胞白血病的发展中发挥重要作用。Tax诱导白血病发生的分子机制尚未阐明。我们使用白细胞介素-2(IL-2)依赖的人类T细胞系(Kit 225)分析了Tax在细胞周期中的功能,该细胞系在缺乏IL-2时可在G(0)/G(1)期发生细胞周期停滞。Tax在IL-2饥饿的Kit 225细胞中激活内源性E2F活性,导致参与G(1)到S期转变的基因的E2F位点携带启动子以细胞类型依赖和p16(INK4a)独立的方式被激活。Tax突变体激活E2F的能力与其激活核因子kappaB和AT的能力一致,然而,单独表达核因子kappaB和AT并不能激活E2F,这表明E2F的激活涉及另一条途径。通过重组腺病毒引入Tax可诱导静止的Kit 225细胞的细胞周期进展至G(2)/M期,并伴有内源性细胞周期蛋白D2基因表达。同样,在用植物血凝素预刺激的外周血淋巴细胞中也观察到Tax诱导的细胞周期进展。对Tax突变体的分析无法区分Tax诱导的细胞周期进展和Tax依赖的E2F激活,这表明Tax可能通过激活E2F诱导细胞周期进展。然而,感染表达E2F1的病毒,其足以在血清饥饿的成纤维细胞中诱导S期,但在IL-2饥饿的Kit 225细胞中既不足以激活E2F也不足以促进细胞周期进展,这意味着Tax激活的T细胞中E2F激活和细胞周期进展存在差异调节。

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