Transcription enhances AID-mediated cytidine deamination by exposing single-stranded DNA on the nontemplate strand

Somatic hypermutation and class switch recombination are DNA modification reactions that alter the genes encoding antibodies in B lymphocytes. Both of these distinct reactions require activation-induced deaminase (AID) and transcription. Here we show that in Escherichia coli , as in eukaryotic cells...

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Bibliographic Details
Published in:Nature immunology Vol. 4; no. 5; pp. 452 - 456
Main Authors: Ramiro, Almudena R., Stavropoulos, Pete, Jankovic, Mila, Nussenzweig, Michel C.
Format: Journal Article
Language:English
Published: New York Nature Publishing Group US 01.05.2003
Nature Publishing Group
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ISSN:1529-2908, 1529-2916
Online Access:Get full text
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Summary:Somatic hypermutation and class switch recombination are DNA modification reactions that alter the genes encoding antibodies in B lymphocytes. Both of these distinct reactions require activation-induced deaminase (AID) and transcription. Here we show that in Escherichia coli , as in eukaryotic cells, the mutation frequency is directly proportional to the transcription of target genes. Transcription enhances mutation of the nontemplate DNA strand, which is exposed as single-stranded DNA during the elongation reaction, but not mutation of the template DNA strand, which is protected by E. coli RNA polymerase. Our results establish a direct link between AID and transcription and suggest that the role of transcription in facilitating mutation is to provide AID with access to single-stranded DNA.
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ISSN:1529-2908
1529-2916
DOI:10.1038/ni920