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Cutting Edge: The Transcription Factor Sox2 Regulates AID Expression in Class-Switched B Cells
Author(s) -
Lauren J. DiMenna,
Wei-Feng Yen,
Laura Nicolás,
Rahul Sharma,
Zara N Saldanha,
Jayanta Chaudhuri
Publication year - 2017
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1502266
Subject(s) - transcription factor , microbiology and biotechnology , class (philosophy) , sox2 , enhanced data rates for gsm evolution , biology , genetics , computer science , gene , telecommunications , artificial intelligence
IgH class switch recombination (CSR) occurs through the deliberate introduction of activation-induced cytidine deaminase (AID)-instigated DNA double-strand breaks into the IgH loci. Because double-strand breaks are generally highly toxic, mechanisms that regulate AID expression are of much relevance to CSR and genomic integrity; however, effectors of such regulatory processes are still poorly understood. In this article, we show that the transcription factor sex determining region Y-box 2 (Sox2) is expressed in activated B cells, but almost exclusively in those that have undergone CSR. We demonstrate that enforced expression of Sox2 in splenic B cells severely inhibits AID expression and CSR, whereas deletion of Sox2 increases the frequency of IgH:c-Myc translocations. These results suggest that Sox2 may regulate AID expression in class-switched B cells to suppress genomic instability associated with CSR.

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