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转录通过在非模板链上暴露单链DNA来增强AID介导的胞嘧啶脱氨作用。

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

作者信息

Ramiro Almudena R, Stavropoulos Pete, Jankovic Mila, Nussenzweig Michel C

机构信息

Laboratory of Molecular Immunology, Rockefeller University, New York, NY 10021, USA.

出版信息

Nat Immunol. 2003 May;4(5):452-6. doi: 10.1038/ni920.

Abstract

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.

摘要

体细胞高频突变和类别转换重组是改变B淋巴细胞中编码抗体基因的DNA修饰反应。这两种不同的反应都需要激活诱导脱氨酶(AID)和转录。我们在此表明,在大肠杆菌中,与真核细胞一样,突变频率与靶基因的转录直接相关。转录增强了非模板DNA链的突变,该链在延伸反应中作为单链DNA暴露,但不增强模板DNA链的突变,模板DNA链受到大肠杆菌RNA聚合酶的保护。我们的结果建立了AID与转录之间的直接联系,并表明转录在促进突变中的作用是为AID提供接触单链DNA的机会。

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