Key result
Activation induced cytidine deaminase (AID) is an essential enzyme that regulates class switch recombination, somatic hypermutation, and gene conversion of the immunoglobulin gene.
This review highlights the dual role of Activation induced cytidine deaminase (AID) in essential immune regulation and potential genome instability.
Supports AID's established role in humoral immunity; leaves open its off-target genomic effects for further study.
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.
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Honjo et al. (2006) conducted a review in Immune system regulation and genome instability. Activation induced cytidine deaminase (AID) was evaluated. Activation induced cytidine deaminase (AID) is an essential enzyme that regulates class switch recombination, somatic hypermutation, and gene conversion of the immunoglobulin gene.
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