丙型肝炎病毒核心蛋白反式抑制基因表达。

D W Kim, R Suzuki, T Harada, I Saito, T Miyamura
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引用次数: 65

摘要

我们已经证明截断的C端疏水结构域缺失的丙型肝炎(HCV)核心蛋白易位到转染细胞的细胞核中(22)。在这项研究中,完整的和截断的HCV核心蛋白在人肝母细胞瘤细胞系HepG2中短暂表达,并检测了它们对病毒和细胞启动子驱动的氯苯乙基转移酶(CAT)基因表达的影响。完整的22 kDa核心蛋白定位于转染细胞的细胞质中,抑制了所有启动子的表达。它们是SV40早期区域、c-fos癌基因、视网膜母细胞瘤易感基因、β -干扰素基因和β -肌动蛋白基因的启动子。相反,位于细胞核的截断的HCV核心蛋白没有表现出这种抑制活性。HCV核心蛋白似乎不仅作为病毒结构蛋白,而且作为基因表达的调节因子,它可能作为细胞基因表达的抑制因子。
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Trans-suppression of gene expression by hepatitis C viral core protein.

We have demonstrated that the truncated hepatitis C (HCV) core protein with its C-terminal hydrophobic domains deleted is translocated to the nucleus of transfected cells (22). In this study, intact and truncated core proteins of HCV were transiently expressed in a human hepatoblastoma cell line, HepG2, and their effects on the expression of the chloramphenycol acethyl transferase (CAT) gene driven by viral and cellular promoters were examined. The intact core protein of 22 kDa which is localized in the cytoplasm of the transfected cells suppressed the expression in all of the promoters tested. They were promoters of the SV40 early region, the c-fos oncogene, the retinoblastoma susceptibility gene, the beta-interferon gene and the beta-actin gene. In contrast, the truncated HCV core protein located in the nucleus did not show such a suppressive activity. The HCV core protein appears to function not only as a viral structural protein but as a regulator of gene expression and it might act as a suppressive factor for the cellular gene expression.

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