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由人类嗜T淋巴细胞病毒1型Tax蛋白诱导的全基因组表达变化:MLK-3混合谱系激酶参与Tax介导的核因子κB激活的证据。

Genome-wide expression changes induced by HTLV-1 Tax: evidence for MLK-3 mixed lineage kinase involvement in Tax-mediated NF-kappaB activation.

作者信息

Ng P W, Iha H, Iwanaga Y, Bittner M, Chen Y, Jiang Y, Gooden G, Trent J M, Meltzer P, Jeang K T, Zeichner S L

机构信息

HIV and AIDS Malignancy Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Oncogene. 2001 Jul 27;20(33):4484-96. doi: 10.1038/sj.onc.1204513.

Abstract

The Tax protein of human T-lymphotropic virus type 1 (HTLV-1), an oncoprotein that transactivates viral and cellular genes, plays a key role in HTLV-1 replication and pathogenesis. We used cDNA microarrays to examine Tax-mediated transcriptional changes in the human Jurkat T-cell lines JPX-9 and JPX-M which express Tax and Tax-mutant protein, respectively, under the control of an inducible promoter. Approximately 300 of the over 2000 genes examined were differentially expressed in the presence of Tax. These genes were grouped according to their function and are discussed in the context of existing findings in the literature. There was strong agreement between our results and genes previously reported as being Tax-responsive. Genes that were differentially expressed in the presence of Tax included those related to apoptosis, the cell cycle and DNA repair, signaling factors, immune modulators, cytokines and growth factors, and adhesion molecules. Functionally, we provide evidence that one of these genes, the mixed-lineage kinase MLK-3, is involved in Tax-mediated NF-kappa-B signaling. Our current results provide additional insights into Tax-mediated signaling.

摘要

人类嗜T淋巴细胞病毒1型(HTLV-1)的Tax蛋白是一种可反式激活病毒和细胞基因的癌蛋白,在HTLV-1复制和发病机制中起关键作用。我们使用cDNA微阵列来检测在可诱导启动子控制下,分别表达Tax和Tax突变蛋白的人Jurkat T细胞系JPX-9和JPX-M中Tax介导的转录变化。在检测的2000多个基因中,约300个基因在有Tax存在时差异表达。这些基因根据其功能进行分组,并结合文献中的现有发现进行讨论。我们的结果与先前报道的对Tax有反应的基因之间有很强的一致性。在有Tax存在时差异表达的基因包括与细胞凋亡、细胞周期和DNA修复、信号因子、免疫调节剂、细胞因子和生长因子以及黏附分子相关的基因。在功能上,我们提供证据表明这些基因之一,即混合谱系激酶MLK-3,参与Tax介导的核因子κB信号传导。我们目前的结果为Tax介导的信号传导提供了更多见解。

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