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TORC1和TORC2共激活因子是人类1型T细胞白血病病毒长末端重复序列的tax激活所必需的。

TORC1 and TORC2 coactivators are required for tax activation of the human T-cell leukemia virus type 1 long terminal repeats.

作者信息

Siu Yeung-Tung, Chin King-Tung, Siu Kam-Leung, Yee Wai Choy Elizabeth, Jeang Kuan-Teh, Jin Dong-Yan

机构信息

Department of Biochemistry, The University of Hong Kong, 3/F Laboratory Block, Faculty of Medicine Building, 21 Sassoon Road, Pokfulam, Hong Kong.

出版信息

J Virol. 2006 Jul;80(14):7052-9. doi: 10.1128/JVI.00103-06.

Abstract

Human T-cell leukemia virus type 1 (HTLV-1) Tax protein activates viral transcription from the long terminal repeats (LTR). Mechanisms through which Tax activates LTR have been established, but coactivators of this process remain to be identified and characterized. Here we show that all three members of the TORC family of transcriptional regulators are coactivators of Tax for LTR-driven expression. TORC coactivation requires CREB, but not ATF4 or other bZIP factors. Tax physically interacts with TORC1, TORC2, and TORC3 (TORC1/2/3), and the depletion of TORC1/2/3 inhibited Tax activity. TORC coactivation can be further enhanced by transcriptional coactivator p300. In addition, coactivators in the p300 family are required for full activity of Tax independently of TORC1/2/3. Thus, both TORC and p300 families of coactivators are essential for optimal activation of HTLV-1 transcription by Tax.

摘要

人类1型T细胞白血病病毒(HTLV-1)的Tax蛋白可激活来自长末端重复序列(LTR)的病毒转录。Tax激活LTR的机制已明确,但该过程的共激活因子仍有待鉴定和表征。在此我们表明,转录调节因子TORC家族的所有三个成员都是Tax介导LTR驱动表达的共激活因子。TORC的共激活作用需要CREB,但不需要ATF4或其他bZIP因子。Tax与TORC1、TORC2和TORC3(TORC1/2/3)发生物理相互作用,TORC1/2/3的缺失会抑制Tax活性。转录共激活因子p300可进一步增强TORC的共激活作用。此外,p300家族的共激活因子对于Tax的完全活性是必需的,且独立于TORC1/2/3。因此,共激活因子的TORC家族和p300家族对于Tax对HTLV-1转录的最佳激活作用均至关重要。

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