首页> 美国卫生研究院文献>Journal of Virology >XBP-1 a Novel Human T-Lymphotropic Virus Type 1 (HTLV-1) Tax Binding Protein Activates HTLV-1 Basal and Tax-Activated Transcription
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XBP-1 a Novel Human T-Lymphotropic Virus Type 1 (HTLV-1) Tax Binding Protein Activates HTLV-1 Basal and Tax-Activated Transcription

机译:XBP-1一种新型的人类T嗜性病毒1型(HTLV-1)税收绑定蛋白激活HTLV-1基础和税收激活的转录。

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摘要

X-box binding protein 1 (XBP-1), a basic leucine zipper transcription factor, plays a key role in the cellular unfolded protein response (UPR). There are two XBP-1 isoforms in cells, spliced XBP-1S and unspliced XBP-1U. XBP-1U has been shown to bind to the 21-bp Tax-responsive element of the human T-lymphotropic virus type 1 (HTLV-1) long terminal repeat (LTR) in vitro and transactivate HTLV-1 transcription. Here we identify XBP-1S as a transcription activator of HTLV-1. Compared to XBP-1U, XBP-1S demonstrates stronger activating effects on both basal and Tax-activated HTLV-1 transcription in cells. Our results show that both XBP-1S and XBP-1U interact with Tax and bind to the HTLV-1 LTR in vivo. In addition, elevated mRNA levels of the gene for XBP-1 and several UPR genes were detected in the HTLV-1-infected C10/MJ and MT2 T-cell lines, suggesting that HTLV-1 infection may trigger the UPR in host cells. We also identify Tax as a positive regulator of the expression of the gene for XBP-1. Activation of the UPR by tunicamycin showed no effect on the HTLV-1 LTR, suggesting that HTLV-1 transcription is specifically regulated by XBP-1. Collectively, our study demonstrates a novel host-virus interaction between a cellular factor XBP-1 and transcriptional regulation of HTLV-1.
机译:X-box结合蛋白1(XBP-1)是一种基本的亮氨酸拉链转录因子,在细胞未折叠蛋白应答(UPR)中起关键作用。细胞中有两种XBP-1亚型,剪接的XBP-1S和未剪接的XBP-1U。 XBP-1U已显示在体​​外与人T型淋巴病毒1型(HTLV-1)长末端重复序列(LTR)的21 bp Tax-respond元件结合并反激活HTLV-1转录。在这里,我们将XBP-1S鉴定为HTLV-1的转录激活因子。与XBP-1U相比,XBP-1S对细胞中的基础和税基活化HTLV-1转录均显示出更强的活化作用。我们的结果表明XBP-1S和XBP-1U都与Tax相互作用,并在体内与HTLV-1 LTR结合。此外,在感染HTLV-1的C10 / MJ和MT2 T细胞系中检测到XBP-1基因和几个UPR基因的mRNA水平升高,表明HTLV-1感染可能触发宿主细胞中的UPR。我们还确定Tax为XBP-1基因表达的正调节剂。衣霉素对UPR的激活未显示对HTLV-1 LTR的影响,这表明HTLV-1转录受XBP-1特异性调节。总的来说,我们的研究表明细胞因子XBP-1和HTLV-1的转录调控之间新型的宿主病毒相互作用。

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