Molecular Mechanisms of Antibody Somatic Hypermutation
Montreal Clinical Research Institute · MRC Laboratory of Molecular Biology
Abstract
Functional antibody genes are assembled by V-D-J joining and then diversified by somatic hypermutation. This hypermutation results from stepwise incorporation of single nucleotide substitutions into the V gene, underpinning much of antibody diversity and affinity maturation. Hypermutation is triggered by activation-induced deaminase (AID), an enzyme which catalyzes targeted deamination of deoxycytidine residues in DNA. The pathways used for processing the AID-generated U:G lesions determine the variety of base substitutions observed during somatic hypermutation. Thus, DNA replication across the uracil yields transition mutations at C:G pairs, whereas uracil excision by UNG uracil-DNA glycosylase creates abasic…
Citation impact
- FWCI
- 22.27
- Percentile
- 100%
- References
- 142
Authors
2Topics & keywords
- Somatic hypermutation
- Uracil-DNA glycosylase
- Deamination
- Immunoglobulin class switching
- Biology
- Cytidine deaminase
- Base excision repair
- Immunoglobulin gene