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通过引入体细胞DNA改变来辅助克服基因组信息的局限性。

AID to overcome the limitations of genomic information by introducing somatic DNA alterations.

作者信息

Honjo Tasuku, Muramatsu Masamichi, Nagaoka Hitoshi, Kinoshita Kazuo, Shinkura Reiko

机构信息

Department of Immunology and Genomic Medicine Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Proc Jpn Acad Ser B Phys Biol Sci. 2006 May;82(3):104-20. doi: 10.2183/pjab.82.104.

Abstract

The immune system has adopted somatic DNA alterations to overcome the limitations of the genomic information. Activation induced cytidine deaminase (AID) is an essential enzyme to regulate class switch recombination (CSR), somatic hypermutation (SHM) and gene conversion (GC) of the immunoglobulin gene. AID is known to be required for DNA cleavage of S regions in CSR and V regions in SHM. However, its molecular mechanism is a focus of extensive debate. RNA editing hypothesis postulates that AID edits yet unknown mRNA, to generate specific endonucleases for CSR and SHM. By contrast, DNA deamination hypothesis assumes that AID deaminates cytosine in DNA, followed by DNA cleavage by base excision repair enzymes. We summarize the basic knowledge for molecular mechanisms for CSR and SHM and then discuss the importance of AID not only in the immune regulation but also in the genome instability.

摘要

免疫系统采用体细胞DNA改变来克服基因组信息的局限性。激活诱导胞嘧啶脱氨酶(AID)是调节免疫球蛋白基因的类别转换重排(CSR)、体细胞高频突变(SHM)和基因转换(GC)的关键酶。已知AID是CSR中S区域和SHM中V区域DNA切割所必需的。然而,其分子机制是广泛争论的焦点。RNA编辑假说假定AID编辑未知的mRNA,以产生用于CSR和SHM的特定内切核酸酶。相比之下,DNA脱氨基假说认为AID使DNA中的胞嘧啶脱氨基,随后由碱基切除修复酶进行DNA切割。我们总结了CSR和SHM分子机制的基础知识,然后讨论了AID不仅在免疫调节中而且在基因组不稳定性中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b103/4323042/e4f2ba57dd2f/82_104f1.jpg

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