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Involvement of the Oncoprotein c-Myc in Viral Telomerase RNA Gene Regulation during Mareks Disease Virus-Induced Lymphomagenesis

机译:癌蛋白c-Myc在马立克氏病病毒诱导的淋巴瘤发生过程中参与病毒端粒酶RNA基因调控。

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摘要

Marek's disease virus (MDV) is an alphaherpesvirus that induces a highly malignant T-lymphoma in chickens. The viral genome encodes two identical copies of a viral telomerase RNA subunit (vTR) that exhibits 88% sequence identity to its chicken ortholog chTR. The minimal telomerase ribonucleoprotein complex consists of a protein subunit with reverse transcriptase activity (TERT) and an RNA subunit (TR). The active complex compensates for the progressive telomere shortening that occurs during mitosis and is involved in the cell immortalization process. We show here that the upregulation of telomerase activity is associated with an increase in vTR gene expression in chickens infected with the highly oncogenic MDV strain RB-1B. A comparative functional analysis of the viral and chicken TR promoters, based on luciferase reporter assays, revealed that the vTR promoter was up to threefold more efficient than the chTR promoter in avian cells. We demonstrated, by directed mutagenesis of the vTR promoter region, that the stronger transcriptional activity of the vTR promoter resulted largely from an E-box located two nucleotides downstream from the transcriptional start site of the vTR gene. Furthermore, transactivation assays and chromatin immunoprecipitation assays demonstrated the involvement of the c-Myc oncoprotein in the transcriptional regulation of vTR. Finally, an Ets binding site was specifically implicated in the transcriptional regulation of vTR in the MDV-transformed lymphoblastoid cell line MSB-1.
机译:马立克氏病病毒(MDV)是一种α疱疹病毒,可在鸡体内诱发高度恶性的T淋巴瘤。病毒基因组编码两个相同拷贝的病毒端粒酶RNA亚基(vTR),与其鸡直系同源基因chTR表现出88%的序列同一性。最小端粒酶核糖核蛋白复合物由具有逆转录酶活性的蛋白亚基(TERT)和RNA亚基(TR)组成。活性复合物补偿有丝分裂期间发生的渐进性端粒缩短,并参与细胞永生化过程。我们在这里显示端粒酶活性的上调与感染高致癌性MDV株RB-1B的鸡中vTR基因表达的增加有关。根据萤光素酶报告基因分析对病毒和鸡TR启动子进行的功能比较分析表明,vTR启动子在禽类细胞中的效率比chTR启动子高三倍。通过对vTR启动子区域的定向诱变,我们证明了vTR启动子的更强转录活性主要是由位于vTR基因转录起始位点下游两个核苷酸的E-box引起的。此外,反式激活试验和染色质免疫沉淀试验证明了c-Myc癌蛋白参与vTR的转录调控。最后,Ets结合位点特别涉及MDV转化的淋巴母细胞样细胞系MSB-1中vTR的转录调控。

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