reviewAnnual Review of BiochemistryFeb 9, 2007Closed access

Molecular Mechanisms of Antibody Somatic Hypermutation

Montreal Clinical Research Institute · MRC Laboratory of Molecular Biology

PubMed
Indexed incrossrefpubmed

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

1,090
total citations
FWCI
22.27
Percentile
100%
References
142
Citations per year

Authors

2

Topics & keywords

Keywords
  • Somatic hypermutation
  • Uracil-DNA glycosylase
  • Deamination
  • Immunoglobulin class switching
  • Biology
  • Cytidine deaminase
  • Base excision repair
  • Immunoglobulin gene
No related works found for this paper.