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V H replacement in rearranged immunoglobulin genes
Author(s) -
Darlow John M.,
Stott David I.
Publication year - 2005
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/j.1365-2567.2004.02084.x
Subject(s) - cytidine deaminase , activation induced (cytidine) deaminase , gene , biology , recombination , genetics , polymerase chain reaction , microbiology and biotechnology , computational biology , antibody , immunoglobulin class switching , b cell
Summary Examples suggesting that all or part of the V H segment of a rearranged V H DJ H may be replaced by all or part of another V H have been appearing since the 1980s. Evidence has been presented of two rather different types of replacement. One of these has gained acceptance and has now been clearly demonstrated to occur. The other, proposed more recently, has not yet gained general acceptance because the same effect can be produced by polymerase chain reaction artefact. We review both types of replacement including a critical examination of evidence for the latter. The first type involves RAG proteins and recombination signal sequences (RSS) and occurs in immature B cells. The second was also thought to be brought about by RAG proteins and RSS. However, it has been reported in hypermutating cells which are not thought to express RAG proteins but in which activation‐induced cytidine deaminase (AID) has recently been shown to initiate homologous recombination. Re‐examination of the published sequences reveals AID target sites in V H ‐V H junction regions and examples that resemble gene conversion.