Effects of APOBEC3G's Cytidine Deaminase Activity on Retroviral Evolution

Mary-Benedicta Obikili
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Abstract

Apolipoprotein B editing complex (APOBEC3/A3) genes are found in mammalian cells. In primates, there are 7 APOBEC3 genes, namely, 3A, 3B, 3C, 3DE, 3F, 3G, and 3H. Previous research has shown that A3 proteins help to inhibit viral infection via their cytidine deaminase activity. However, it has also been found that A3 proteins could also lead to viral evolution, where viruses such as HIV (Human Immunodeficiency Virus) instead gain beneficial mutations that enable them to overcome the antiviral activity of A3 proteins, gain resistance to certain drugs used for treating viral infections and escape recognition by the immune system. This paper is a review article summarizing the role of A3G on viral infection and evolution, and the potential impact viral evolution could have in treatment of retroviral infections such as HIV.
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APOBEC3G胞苷脱氨酶活性对逆转录病毒进化的影响
载脂蛋白B编辑复合物(APOBEC3/A3)基因存在于哺乳动物细胞中。在灵长类动物中,APOBEC3基因有7个,分别是3A、3B、3C、3DE、3F、3G和3H。先前的研究表明,A3蛋白通过胞苷脱氨酶活性帮助抑制病毒感染。然而,也发现A3蛋白也可能导致病毒进化,HIV(人类免疫缺陷病毒)等病毒反而获得有益的突变,使它们能够克服A3蛋白的抗病毒活性,获得对某些用于治疗病毒感染的药物的抗性,并逃避免疫系统的识别。本文综述了A3G在病毒感染和进化中的作用,以及病毒进化对治疗HIV等逆转录病毒感染的潜在影响。
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