Direct Repression of <i>prdm1</i> by Bcl-6 Inhibits Plasmacytic Differentiation

Chainarong Tunyaplin(Columbia University), Arthur L. Shaffer(National Cancer Institute), Cristina Angelin‐Duclos(Columbia University), Xin Yu(National Cancer Institute), Louis M. Staudt(National Cancer Institute), Kathryn Calame(Columbia University)
The Journal of Immunology
July 1, 2004
Cited by 361

Abstract

We have identified two intronic regions of mouse prdm1, the gene encoding B lymphocyte-induced maturation protein-1 (Blimp-1), which confer transcriptional repression in response to Bcl-6. The Bcl-6 response element in intron 5, which is conserved between mice and humans, was studied in detail. It binds Bcl-6 in vitro and was shown by chromatin immunoprecipitation to be occupied by Bcl-6 in vivo. Neither Bcl-6 response element functions as a STAT3-response element, showing that STAT3 does not compete with Bcl-6 at these sites. Bcl-6(-/-) mice confirm the biological importance of Bcl-6-dependent repression of prdm1. These mice have elevated Ab response, increased Ig-secreting cells, and increased Blimp-1(+) cells in spleen following immunization and their splenic B cells show accelerated plasmacytic development in vitro.


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