Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Cell Cycle. 2012 Jan 1;11(1):33-8. doi: 10.4161/cc.11.1.18706.
The human APOBEC3 family of cytidine deaminases constitutes a cellular intrinsic defense mechanism that is effective against a range of viruses and retro-elements. While it is well established that these enzymes are powerful mutators of viral DNA, the possibility that their activity could threaten the integrity of the host genome has only recently begun to be investigated. Here, we discuss the implications of new evidence suggesting that APOBEC3 proteins can mediate the deamination of cellular DNA. The maintenance of genomic integrity in the face of this potential off-target activity must require high fidelity DNA repair and strict regulation of APOBEC3 gene expression and enzyme activity. Conversely, the ability of specific members of the APOBEC3 family to activate DNA damage signaling pathways might also reflect another way that these proteins contribute to the host immune response.
人类 APOBEC3 家族的胞嘧啶脱氨酶构成了一种细胞内在的防御机制,对多种病毒和反转录元件有效。虽然这些酶是病毒 DNA 的强大诱变剂已经得到了很好的证实,但它们的活性可能会威胁到宿主基因组的完整性这一可能性最近才开始被研究。在这里,我们讨论了新证据表明 APOBEC3 蛋白可以介导细胞 DNA 的脱氨作用的意义。面对这种潜在的非靶标活性,基因组完整性的维持必须需要高保真度的 DNA 修复以及对 APOBEC3 基因表达和酶活性的严格调控。相反,APOBEC3 家族的特定成员激活 DNA 损伤信号通路的能力也可能反映了这些蛋白质有助于宿主免疫反应的另一种方式。