| Literature DB >> 29038163 |
Baeck-Seung Lee1,2, Bum-Kyu Lee1,2, Vishwanath R Iyer1,2, Barry P Sleckman3, Arthur L Shaffer4, Gregory C Ippolito1,2, Haley O Tucker5,2, Joseph D Dekker5,2.
Abstract
Recombination activating gene 1 (RAG1) and RAG2 are critical enzymes for initiating variable-diversity-joining [V(D)J] segment recombination, an essential process for antigen receptor expression and lymphocyte development. The BCL11A transcription factor is required for B cell and plasmacytoid dendritic cell (pDC) development, but its molecular function(s) in early B cell fate specification and commitment is unknown. We show here that the major B cell isoform, BCL11A-XL, binds directly to the RAG1 promoter as well as directly to regulatory regions of transcription factors previously implicated in both B cell and pDC development to activate RAG1 and RAG2 gene transcription in pro- and pre-B cells. We employed BCL11A overexpression with recombination substrates to demonstrate direct consequences of BCL11A/RAG modulation on V(D)J recombination. We conclude that BCL11A is a critical component of a transcriptional network that regulates B cell fate by controlling V(D)J recombination.Entities:
Keywords: B cell development; Bcl11a; RAG; V(D)J; immunology
Year: 2017 PMID: 29038163 PMCID: PMC5730723 DOI: 10.1128/MCB.00362-17
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272