Cascalho Marilia
Transplantation Biology, and Departments of Immunology, Surgery, and Pediatrics, Mayo Clinic, Rochester, MN 55905, USA.
J Immunol. 2004 Jun 1;172(11):6513-8. doi: 10.4049/jimmunol.172.11.6513.
Cytidine deamination of nucleic acids underlies diversification of Ig genes and inhibition of retroviral infection, and thus, it would appear to be vital to host defense. The host defense properties of cytidine deamination require two distinct but homologous cytidine deaminases-activation-induced cytidine deaminase and apolipoprotein B-editing cytidine deaminase, subunit 3G. Although cytidine deamination has clear benefits, it might well have biological costs. Uncontrolled cytidine deamination might generate misfolded polypeptides, dominant-negative proteins, or mutations in tumor suppressor genes, and thus contribute to tumor formation. How cytidine deaminases target a given nucleic acid substrate at specific sequences is not understood, and what protects cells from uncontrolled mutagenesis is not known. In this paper, I shall review the functions and regulation of activation-induced cytidine deaminase and apolipoprotein B-editing cytidine deaminase, subunit 3G, and speculate about the basis for site specificity vis-à-vis generalized mutagenesis.
核酸的胞苷脱氨作用是免疫球蛋白基因多样化及逆转录病毒感染受抑制的基础,因此,它似乎对宿主防御至关重要。胞苷脱氨作用的宿主防御特性需要两种不同但同源的胞苷脱氨酶——活化诱导胞苷脱氨酶和载脂蛋白B编辑胞苷脱氨酶3G亚基。尽管胞苷脱氨作用有明显益处,但它很可能也有生物学代价。不受控制的胞苷脱氨作用可能产生错误折叠的多肽、显性负性蛋白或肿瘤抑制基因中的突变,从而促进肿瘤形成。胞苷脱氨酶如何在特定序列靶向给定的核酸底物尚不清楚,以及什么保护细胞免受不受控制的诱变也未知。在本文中,我将综述活化诱导胞苷脱氨酶和载脂蛋白B编辑胞苷脱氨酶3G亚基的功能和调控,并推测位点特异性相对于普遍诱变的基础。