A novel Pax5-binding regulatory element in the Igk locus

Rena Levin-Klein, Andrei Kirillov, Chaggai Rosenbluh, Howard Cedar, Yehudit Bergman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The Igk locus undergoes a variety of different molecular processes during B cell development, including V(D)J rearrangement and somatic hypermutations (SHM), which are influenced by cis regulatory regions (RRs) within the locus. The Igk locus includes three characterized RRs termed the intronic (iEk), 3'Ek, and Ed enhancers. We had previously noted that a region of DNA upstream of the iEk and matrix attachment region (MAR) was necessary for demethylation of the locus in cell culture. In this study, we further characterized this region, which we have termed Dm, for demethylation element. Pre-rearranged Igk transgenes containing a deletion of the entire Dm region, or of a Pax5-binding site within the region, fail to undergo efficient CpG demethylation in mature B cells in vivo. Furthermore, we generated mice with a deletion of the full Dm region at the endogenous Igk locus. The most prominent phenotype of these mice is reduced SHM in germinal center B cells in Peyer's patches. In conclusion, we propose the Dm element as a novel Pax5-binding cis regulatory element, which works in concert with the known enhancers, and plays a role in Igk demethylation and SHM.

Original languageAmerican English
Article numberArticle 240
JournalFrontiers in Immunology
Volume5
Issue numberMAY
DOIs
StatePublished - 2014

Keywords

  • B cell development
  • DNA methylation
  • Pax5
  • Somatic hypermutation
  • V(D)J rearrangement

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