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BATF regulates the expression of Nfil3, Wnt10a and miR155hg for efficient induction of antibody class switch recombination in mice.

Rosemary E Morman | Patrick G Schweickert | Stephen F Konieczny | Elizabeth J Taparowsky
European journal of immunology | 2018

BATF functions in T cells and B cells to control the host response to antigen and promote the production of class switched immunoglobulins. In this study, we demonstrate that BATF expression increases rapidly, and transiently, following B cell stimulation and use an inducible murine model of BATF deletion to show that this induction is necessary, and sufficient, for immunoglobulin (Ig) class switch recombination (CSR). We examine two genes (Nfil3 and miR155gh) that are positively regulated, and one gene (Wnt10a) that is negatively regulated by BATF during CSR. These genes play essential roles in CSR and each impacts the expression and/or function of the others. Our observations allow these targets of BATF regulation to be positioned in a network upstream of the activation of germline transcripts (GLT) from the IgH locus and of transcriptional activation of Aicda - the gene encoding the enzyme directing Ig gene rearrangements. This work extends the knowledge of the molecular control of CSR and, importantly, positions the induction and function of BATF as an early event in this process.

Pubmed ID: 29898247

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: NIH P30 CA023168
  • Agency: NIH HHS, United States
    Id: S10 OD020029
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001108
  • Agency: NCATS NIH HHS, United States
    Id: NIH UL1 TR002529
  • Agency: NCI NIH HHS, United States
    Id: P30 CA023168
  • Agency: NCATS NIH HHS, United States
    Id: TL1 TR001107
  • Agency: NIAID NIH HHS, United States
    Id: R21 AI105620

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