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人 2',5'-寡聚腺苷酸合成酶家族成员依赖核糖核酸酶 L 的抗丙型肝炎病毒作用。

The ribonuclease L-dependent antiviral roles of human 2',5'-oligoadenylate synthetase family members against hepatitis C virus.

机构信息

School of Life Sciences and Biotechnology, Korea University, Anam-dong 5-1, Seoul 136-701, Republic of Korea.

出版信息

FEBS Lett. 2013 Jan 16;587(2):156-64. doi: 10.1016/j.febslet.2012.11.010. Epub 2012 Nov 26.

Abstract

The latent ribonuclease RNase L and the interferon-inducible 2',5'-oligoadenylate synthetase (OAS) have been implicated in the antiviral response against hepatitis C virus (HCV). However, the specific roles of these enzymes against HCV have not been fully elucidated. In this study, a scarce endogenous expression and RNA degrading activity of RNase L in human hepatoma Huh7 cells enabled us to demonstrate the antiviral activity of RNase L against HCV replication through the transient expression of the enzyme. The antiviral potential of specific members of the OAS family was further examined through overexpression and RNA interference approaches. Our data suggested that among the members of the OAS family, OAS1 p46 and OAS3 p100 mediate the RNase L-dependent antiviral activity against HCV.

摘要

潜伏核糖核酸酶 RNase L 和干扰素诱导的 2',5'-寡聚腺苷酸合成酶 (OAS) 已被牵连到针对丙型肝炎病毒 (HCV) 的抗病毒反应中。然而,这些酶针对 HCV 的具体作用尚未完全阐明。在这项研究中,人肝癌 Huh7 细胞中 RNase L 的稀少内源性表达和 RNA 降解活性使我们能够通过酶的瞬时表达来证明 RNase L 对 HCV 复制的抗病毒活性。通过过表达和 RNA 干扰方法进一步研究了 OAS 家族的特定成员的抗病毒潜力。我们的数据表明,在 OAS 家族的成员中,OAS1 p46 和 OAS3 p100 介导了 RNase L 依赖的针对 HCV 的抗病毒活性。

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