Distinct viral determinants for the packaging of human cytidine deaminases APOBEC3G and APOBEC3C.
Distinct viral determinants for the packaging of human cytidine deaminases APOBEC3G and APOBEC3C.
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DOI：
10.1016/j.virol.2008.04.012
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发表时间：
2008-07
期刊：
影响因子：
3.7
通讯作者：
Tao Wang;Wenyan Zhang;C. Tian;Bindong Liu;Yunkai Yu;Lingmei Ding;P. Spearman;Xiao-Fang Yu
中科院分区：
文献类型：
--
作者：
Tao Wang;Wenyan Zhang;C. Tian;Bindong Liu;Yunkai Yu;Lingmei Ding;P. Spearman;Xiao-Fang Yu
Human APOBEC3G and other APOBEC3 cytidine deaminases inhibit a variety of retroviruses, including Vif-deficient HIV-1. These host proteins are packaged into viral particles and inhibit the replication of virus in new target cells. A3G and A3F are known to be efficiently packaged into HIV-1 virions by binding to 7SL RNA through the Gag NC domain; however, the packaging mechanisms of other APOBEC3 proteins are poorly defined. We have now demonstrated that APOBEC3C (A3C) can be efficiently packaged into HIV-1 virions that are deficient for viral genomic RNA. Inhibition of the encapsidation of 7SL RNA into HIV-1 virions blocked the packaging of A3G, but not A3C. While the NC domain is required for efficient packaging of A3G, deletion of this domain had little effect on A3C packaging into HIV-1 Gag particles. A3C interacted with HIV-1 Gag which was MA domain-dependent and RNA-dependent. Deletion of the MA domain of HIV-1 Gag inhibited A3C but not A3G packaging into HIV-1 Gag particles. Thus, A3G and A3C have evolved to use distinct mechanisms for targeting retroviruses.
