朱艳萍, 蒋建东, 彭宗根. APOBEC3G抑制病毒复制作用机制研究进展J. 药学学报, 2014,49(1): 30-36.
引用本文: 朱艳萍, 蒋建东, 彭宗根. APOBEC3G抑制病毒复制作用机制研究进展J. 药学学报, 2014,49(1): 30-36.
ZHU Yan-ping, JIANG Jian-dong, PENG Zong-gen. Recent advances in the study of mechanism of APOBEC3G against virusJ. Acta Pharmaceutica Sinica, 2014,49(1): 30-36.
Citation: ZHU Yan-ping, JIANG Jian-dong, PENG Zong-gen. Recent advances in the study of mechanism of APOBEC3G against virusJ. Acta Pharmaceutica Sinica, 2014,49(1): 30-36.

APOBEC3G抑制病毒复制作用机制研究进展

Recent advances in the study of mechanism of APOBEC3G against virus

  • 摘要: APOBEC3家族是近年发现的具有脱氨基作用的一类胞苷脱氨酶,APOBEC3G是其家族成员之一,被认为是机体固有免疫家族的新成员,其发现开拓了病毒学领域固有免疫防御机制研究的新方向。APOBEC3G具有抑制多种病毒复制的活性,其机制或通过脱氨基作用引起病毒基因组超突变,或通过非脱氨基依赖的其他复杂机制,作用于病毒的逆转录、复制以及核壳化等生命周期的多个阶段。但病毒会编码病毒蛋白,导致APOBEC3G的抑制病毒复制作用减弱。深入研究APOBEC3G与病毒的相互作用有利于新型抗病毒药物的研发。

     

    Abstract: APOBEC3 is a class of cytidine deaminase, which is considered as a new member of the innate immune system, and APOBEC3G belongs to this family. The research about APOBEC3G is a new direction of innate immune defense mechanism against virus. APOBEC3G has the restrictive activity on many viral replications, which deaminates dC to dU in the viral genome and then induces extensive hypermutation. APOBEC3G can also interrupt viral replication at several phases such as reverse transcription, replication, nucleocapsid and so on by non-deamination mechanisms. However, virus can encode viral proteins to counteract the restriction activity of APOBEC3G. Elucidation of the antagonistic interaction between APOBEC3G and the virus will be contributed to development of new antiviral drugs in the future.

     

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