Rbm15 Modulates Notch-Induced Transcriptional Activation and Affects Myeloid Differentiation

Abstract

RBM15 is the fusion partner with MKL in the t(1;22) translocation of acute megakaryoblastic leukemia. To understand the role of the RBM15-MKL1 fusion protein in leukemia, we must understand the normal functions of RBM15 and MKL. Here, we show a role for Rbm15 in myelopoiesis. Rbm15 is expressed at highest levels in hematopoietic stem cells and at more moderate levels during myelopoiesis of murine cell lines and primary murine cells. Decreasing Rbm15 levels with RNA interference enhances differentiation of the 32DWT18 myeloid precursor cell line. Conversely, enforced expression of Rbm15 inhibits 32DWT18 differentiation. We show that Rbm15 alters Notch-induced HES1 promoter activity in a cell type-specific manner. Rbm15 inhibits Notch-induced HES1 transcription in nonhematopoietic cells but stimulates this activity in hematopoietic cell lines, including 32DWT18 and human erythroleukemia cells. Moreover, the N terminus of Rbm15 coimmunoprecipitates with RBPJκ, a critical factor in Notch signaling, and the Rbm15 N terminus has a dominant negative effect, impairing activation of HES1 promoter activity by full-length-Rbm15. Thus, Rbm15 is differentially expressed during hematopoiesis and may act to inhibit myeloid differentiation in hematopoietic cells via a mechanism that is mediated by stimulation of Notch signaling via RBPJκ.

SUPPLEMENTAL MATERIAL

This work was supported by NIH grants HL63357, DK0724429, and DK053037 and by St. Jude Cancer Center CORE grant CA21765 (to C.N. and S.W.M.); the Children's Leukemia Research Association, Inc.; the Leukemia Lymphoma Foundation; and the American Lebanese Syrian Associated Charities, St. Jude Children's Research Hospital.

We thank Yuying Ling for generously providing the Flag-RBPJκ expression plasmid; Warren Pear for the MAML retroviral expression plasmid; Xiaoli Cui for excellent experimental assistance; Michael Hodsdon for protein structure analysis; and Justin Cohen, Jiankan Guo, and Robert Harris for many helpful discussions.