首页> 美国卫生研究院文献>Journal of Virology >The human T-cell leukemia virus type 1 transactivator protein Tax colocalizes in unique nuclear structures with NF-kappaB proteins.
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The human T-cell leukemia virus type 1 transactivator protein Tax colocalizes in unique nuclear structures with NF-kappaB proteins.

机译:人类T细胞白血病病毒1型反式激活蛋白Tax与NF-κB蛋白共定位在独特的核结构中。

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摘要

The Tax protein of human T-cell leukemia virus type 1 (HTLV-1) is a potent activator of viral transcription. Tax also activates the expression of specific cellular genes involved in the control of T-lymphocyte growth via effects on cellular transcription factors, including members of the NF-kappaB/cRel family. Immunocytochemistry and electron microscopy were used to characterize the intracellular localization of Tax and identify cellular factors which are the potential targets for its transcriptional activity. These studies indicated that Tax localizes in discrete nuclear foci in T lymphocytes transformed by HTLV-1 and in cells transduced with Tax expression vectors. The Tax-containing foci are complex nuclear structures comprising a central core in which Tax colocalizes with splicing factor Sm. In addition to splicing factors Sm and SC-35, the Tax-containing nuclear structures also contain transcriptional components, including the largest subunit of RNA polymerase II and cyclin-dependent kinase CDK8. The inclusion of the two subunits of NF-kappaB, p50 and RelA, and the presence of the mRNA from a gene specifically activated by Tax through NF-kappaB binding sites suggest that these unique nuclear structures participate in Tax-mediated activation of gene expression via the NF-kappaB pathway.
机译:1型人T细胞白血病病毒(HTLV-1)的Tax蛋白是病毒转录的有效激活剂。 Tax还通过影响细胞转录因子(包括NF-kappaB / cRel家族成员)来激活参与T淋巴细胞生长控制的特定细胞基因的表达。免疫细胞化学和电子显微镜用于表征Tax的细胞内定位,并鉴定细胞因子,这些因子是其转录活性的潜在靶标。这些研究表明,Tax定位在由HTLV-1转化的T淋巴细胞和使用Tax表达载体转导的细胞中的离散核灶中。含税病灶是复杂的核结构,包括中央核心,其中,Tax与剪接因子Sm共定位。除剪接因子Sm和SC-35以外,含Tax的核结构还包含转录成分,包括RNA聚合酶II和细胞周期蛋白依赖性激酶CDK8的最大亚基。包含NF-kappaB的两个亚基,p50和RelA,以及存在一个由Tax通过NF-kappAB结合位点特异性激活的基因的mRNA,这表明这些独特的核结构参与了Tax-介导的通过NF-κB途径。

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