4.6 Review Book Chapter

The biochemistry of somatic hypermutation

Journal

ANNUAL REVIEW OF IMMUNOLOGY
Volume 26, Issue -, Pages 481-511

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.immunol.26.021607.090236

Keywords

activation-induced cytidine deaminase (AID, aicda); mismatch repair; antibody diversity; base excision repair; error-prone repair; germinal center

Categories

Funding

  1. NATIONAL CANCER INSTITUTE [R01CA102705, R01CA072649, T32CA009173] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R01ES013192] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007288, R37GM021422] Funding Source: NIH RePORTER
  4. NCI NIH HHS [R01 CA72649, T32 CA B09173, R01CA102705] Funding Source: Medline
  5. NIEHS NIH HHS [ES013192] Funding Source: Medline
  6. NIGMS NIH HHS [T32 GM 007288, R37GM21422] Funding Source: Medline

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Affinity maturation of the Immoral response is mediated by somatic hypermutation of the immunoglobulin (Ig) genes and selection of higher-affinity B cell clones. Activation-induced cytidine deaminase (AID) is the first of a complex series of proteins that introduce these point mutations into variable regions of the Ig genes. AID deaminates deoxycytidine residues in single-stranded DNA to deoxyuridines, which are then processed by DNA replication, base excision repair (BER), or mismatch repair (MMR). In germinal center B cells, MMR, BER, and other factors are diverted from their normal roles in preserving genomic integrity to increase diversity within the Ig locus. Both AID and these components of an emerging error-prone mutasome are regulated on many levels by complex mechanisms that are only beginning to be elucidated.

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