首页> 外文OA文献 >Viral Interferon Regulatory Factor 1 of Kaposi's Sarcoma-Associated Herpesvirus Interacts with a Cell Death Regulator, GRIM19, and Inhibits Interferon/Retinoic Acid-Induced Cell Death
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Viral Interferon Regulatory Factor 1 of Kaposi's Sarcoma-Associated Herpesvirus Interacts with a Cell Death Regulator, GRIM19, and Inhibits Interferon/Retinoic Acid-Induced Cell Death

机译:卡波西氏肉瘤相关疱疹病毒的病毒干扰素调节因子1与细胞死亡调节剂GRIM19相互作用,并抑制干扰素/视黄酸诱导的细胞死亡。

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摘要

Kaposi's sarcoma-associated herpesvirus (KSHV) plays a significant role in the development of Kaposi's sarcoma, primary effusion lymphoma, and some forms of multicentric Castleman's disease. The KSHV open reading frame K9 encodes the viral interferon (IFN) factor 1 (vIRF1), which downregulates IFN- and IRF-mediated transcriptional activation, and leads to cellular transformation in rodent fibroblasts and induction of tumors in nude mice. Using the yeast two-hybrid assay, we identified genes associated with retinoid-IFN-induced mortality-19 (GRIM19), which interacts directly with vIRF1, both in vivo and in vitro. The N-terminal region of vIRF1 is required for binding GRIM19. Colocalization of vIRF1 and GRIM19 was observed in 293T cells. The vIRF1 protein deregulates GRIM19-induced apoptosis in the presence of IFN/all-trans-retinoic acid (RA) and inhibits IFN/RA-induced cell death. Another DNA tumor viral protein, human papillomavirus type 16 E6, also binds GRIM19, suggesting that this is a general target of viral proteins. Our results collectively indicate that vIRF1 modulates IFN/RA-cell death signals via interactions with GRIM19.
机译:卡波西氏肉瘤相关疱疹病毒(KSHV)在卡波西氏肉瘤,原发性渗出性淋巴瘤和某些形式的多中心卡斯曼氏病的发展中起重要作用。 KSHV开放阅读框K9编码病毒干扰素(IFN)因子1(vIRF1),下调IFN和IRF介导的转录激活,并导致啮齿动物成纤维细胞发生细胞转化和裸鼠体内的肿瘤诱导。使用酵母双杂交测定法,我们在体内和体外鉴定了与类维生素A-IFN诱导的死亡率-19(GRIM19)相关的基因,该基因直接与vIRF1相互作用。 vIRF1的N端区域是结合GRIM19所必需的。在293T细胞中观察到vIRF1和GRIM19的共定位。 vIRF1蛋白在存在IFN /全反式维甲酸(RA)的情况下解除GRIM19诱导的细胞凋亡,并抑制IFN / RA诱导的细胞死亡。另一种DNA肿瘤病毒蛋白,人类乳头瘤病毒16 E6型,也结合GRIM19,表明这是病毒蛋白的一般靶标。我们的结果共同表明,vIRF1通过与GRIM19的相互作用调节IFN / RA细胞死亡信号。

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