Aid and mismatch repair in antibody diversification

Alberto Martin, Matthew D. Scharff

Research output: Contribution to journalArticle

101 Citations (Scopus)

Abstract

In response to antigen, B cells undergo a series of specialized genetic events to produce the 'ideal' population of antibodies to prevent and eradicate infections. Although these events - somatic hypermutation, gene conversion and class-switch recombination - have been recognized for many years, the enzymes that are involved have remained elusive. The recent discovery that activation-induced cytidine deaminase (AID) and the mismatch repair (MMR) system are involved in these processes has led to new models of the biochemical events that generate antibody diversity. However, there is still considerable uncertainty about the mechanism of action of AID, and there are differing viewpoints about the role of MMR.

Original languageEnglish (US)
Pages (from-to)605-614
Number of pages10
JournalNature Reviews Immunology
Volume2
Issue number8
StatePublished - Aug 2002

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DNA Mismatch Repair
Antibody Diversity
Gene Conversion
Antibodies
Genetic Recombination
Uncertainty
B-Lymphocytes
Antigens
Enzymes
Infection
Population
AICDA (activation-induced cytidine deaminase)

ASJC Scopus subject areas

  • Immunology

Cite this

Aid and mismatch repair in antibody diversification. / Martin, Alberto; Scharff, Matthew D.

In: Nature Reviews Immunology, Vol. 2, No. 8, 08.2002, p. 605-614.

Research output: Contribution to journalArticle

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