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脱氨基作用导致的死亡:一种针对HIV-1的新型宿主限制系统。

Death by deamination: a novel host restriction system for HIV-1.

作者信息

Goff Stephen P

机构信息

Howard Hughes Medical Institute, Department of Biochemistry and Molecular Biophysics, Columbia University College of Physicians and Surgeons, 701 West 168th Street, New York, NY 10032, USA.

出版信息

Cell. 2003 Aug 8;114(3):281-3. doi: 10.1016/s0092-8674(03)00602-0.

Abstract

A human gene with potent antiretroviral activity has recently been found to encode a new member of the family of cytidine deaminases, previously known to be involved in mRNA editing, immunoglobulin gene class switching, and immunoglobulin gene hypermutation. The enzyme attacks viral DNA as it is synthesized in infected cells and prevents the formation of functional proviruses. The Vif gene of HIV-1 blocks this host restriction and so allows virus replication.

摘要

最近发现一种具有强大抗逆转录病毒活性的人类基因编码胞苷脱氨酶家族的一个新成员,此前已知该家族参与信使核糖核酸编辑、免疫球蛋白基因类别转换和免疫球蛋白基因超突变。这种酶在病毒DNA于受感染细胞中合成时对其进行攻击,阻止功能性前病毒的形成。HIV-1的Vif基因可阻断这种宿主限制,从而使病毒得以复制。

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