Ross T M, Minella A C, Fang Z Y, Pettiford S M, Green P L
Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2363, USA.
J Virol. 1997 Nov;71(11):8912-7. doi: 10.1128/JVI.71.11.8912-8917.1997.
A mutational analysis of human T-cell leukemia virus type 2 (HTLV-2) Tax (Tax-2) was performed to identify regions within Tax-2 important for activation of promoters through the CREB/ATF or NF-kappaB/Rel signaling pathway. Tax-2 mutations within the putative zinc-binding region as well as mutations at the carboxy terminus disrupted CREB/ATF transactivation. A single mutation within the central proline-rich region of Tax-2 disrupted the transactivation of the NF-kappaB/Rel pathway. Surprisingly, this mutation, which is thought to be in a separate activation domain, was suppressed by mutations within or around the putative zinc-binding region, suggesting an interaction between these two regions. These analyses indicate that the functional regions or domains important for transactivation through the CREB/ATF or NF-kappaB/Rel signaling pathway are similar, but not identical, in Tax-1 and Tax-2. Identification of these distinct Tax-2 mutants should facilitate comparative biological studies of HTLV-1 and HTLV-2 and ultimately lead to the determination of the functional importance of Tax trans-acting capacities in T-lymphocyte transformation by HTLV.
对人类2型T细胞白血病病毒(HTLV-2)Tax(Tax-2)进行了突变分析,以确定Tax-2中对于通过CREB/ATF或NF-κB/Rel信号通路激活启动子很重要的区域。推定的锌结合区域内的Tax-2突变以及羧基末端的突变破坏了CREB/ATF反式激活。Tax-2富含脯氨酸的中央区域内的单个突变破坏了NF-κB/Rel途径的反式激活。令人惊讶的是,这个被认为位于一个单独激活域中的突变,被推定的锌结合区域内或其周围的突变所抑制,这表明这两个区域之间存在相互作用。这些分析表明,对于通过CREB/ATF或NF-κB/Rel信号通路进行反式激活很重要的功能区域或结构域在Tax-1和Tax-2中相似但不相同。鉴定这些不同的Tax-2突变体应有助于对HTLV-1和HTLV-2进行比较生物学研究,并最终有助于确定Tax反式作用能力在HTLV诱导的T淋巴细胞转化中的功能重要性。