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Publication : CTCF orchestrates the germinal centre transcriptional program and prevents premature plasma cell differentiation.

First Author  Pérez-García A Year  2017
Journal  Nat Commun Volume  8
Pages  16067 PubMed ID  28677680
Mgi Jnum  J:253153 Mgi Id  MGI:5921081
Doi  10.1038/ncomms16067 Citation  Perez-Garcia A, et al. (2017) CTCF orchestrates the germinal centre transcriptional program and prevents premature plasma cell differentiation. Nat Commun 8:16067
abstractText  In germinal centres (GC) mature B cells undergo intense proliferation and immunoglobulin gene modification before they differentiate into memory B cells or long-lived plasma cells (PC). GC B-cell-to-PC transition involves a major transcriptional switch that promotes a halt in cell proliferation and the production of secreted immunoglobulins. Here we show that the CCCTC-binding factor (CTCF) is required for the GC reaction in vivo, whereas in vitro the requirement for CTCF is not universal and instead depends on the pathways used for B-cell activation. CTCF maintains the GC transcriptional programme, allows a high proliferation rate, and represses the expression of Blimp-1, the master regulator of PC differentiation. Restoration of Blimp-1 levels partially rescues the proliferation defect of CTCF-deficient B cells. Thus, our data reveal an essential function of CTCF in maintaining the GC transcriptional programme and preventing premature PC differentiation.
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