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人类T细胞白血病病毒癌蛋白Tax对IKK-γ寡聚化的刺激作用。

Stimulation of IKK-gamma oligomerization by the human T-cell leukemia virus oncoprotein Tax.

作者信息

Huang Guo Jin, Zhang Zhi Qing, Jin Dong Yan

机构信息

National Key Laboratory for Molecular Virology, Institute of Virology, 100 Yingxin Street, 100052, Beijing, PR China.

出版信息

FEBS Lett. 2002 Nov 20;531(3):494-8. doi: 10.1016/s0014-5793(02)03590-1.

Abstract

Human T-cell leukemia virus type 1 oncoprotein Tax activates NF-kappaB through direct binding to IKK-gamma, the regulatory component of the IkappaB kinase complex. Mechanisms by which IKK-gamma adapts the Tax signal to the IkappaB kinase are poorly understood. Here we demonstrate that IKK-gamma forms homodimer and homotrimer both in vitro and in yeast or mammalian cells through a C-terminal domain comprising amino acids 251-419. In contrast, Tax protein targets a central region of IKK-gamma, which consists of amino acids 201-250. Interestingly, Tax stimulates the oligomerization of IKK-gamma, likely through direct binding. Taken together, our findings suggest a new model of Tax activation of NF-kappaB, in which Tax interacts with IKK-gamma to stimulate its oligomerization.

摘要

人类1型T细胞白血病病毒癌蛋白Tax通过直接结合IκB激酶复合物的调节成分IKK-γ来激活核因子κB(NF-κB)。IKK-γ将Tax信号传递给IκB激酶的机制尚不清楚。在这里,我们证明IKK-γ在体外、酵母或哺乳动物细胞中通过包含251-419位氨基酸的C末端结构域形成同型二聚体和同型三聚体。相比之下,Tax蛋白靶向IKK-γ的一个中心区域,该区域由201-250位氨基酸组成。有趣的是,Tax可能通过直接结合刺激IKK-γ的寡聚化。综上所述,我们的研究结果提示了一种新的Tax激活NF-κB的模型,即Tax与IKK-γ相互作用以刺激其寡聚化。

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