Chd7 deficiency delays leukemogenesis in mice induced by Cbfb-MYH11

Tao Zhen, Erika M. Kwon, Ling Zhao, Jingmei Hsu, R. Katherine Hyde, Ying Lu, Lemlem Alemu, Nancy A. Speck, P. Paul Liu

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


Inversion of chromosome 16 is a consistent finding in patients with acute myeloid leukemia subtype M4 with eosinophilia, which generates a CBFB-MYH11 fusion gene. Previous studies showed that the interaction between CBFb-smooth muscle myosin heavy chain (SMMHC; encoded by CBFB-MYH11) and RUNX1 plays a critical role in the pathogenesis of this leukemia. Recently, it was shown that chromodomain helicase DNA-binding protein-7 (CHD7) interacts with RUNX1 and suppresses RUNX1-induced expansion of hematopoietic stem and progenitor cells. These results suggest that CHD7 is also critical for CBFB-MYH11–induced leukemogenesis. To test this hypothesis, we generated Chd7f/fMx1-CreCbfb1/56M mice, which expressed the Cbfb-MYH11 fusion gene and deactivated Chd7 in hematopoietic cells upon inducing Cre with polyinosinic-polycytidylic acid. The LinSca1c-Kit1 (LK) population was significantly lower in Chd7f/fMx1-CreCbfb1/56M mice than in Mx1-CreCbfb1/56M mice. In addition, there were fewer 5-bromo-29-deoxyuridine–positive cells in the LK population in Chd7f/fMx1-CreCbfb1/56M mice, and genes associated with cell cycle, cell growth, and proliferation were differentially expressed between Chd7f/fMx1-CreCbfb1/56M and Mx1-CreCbfb1/56M leukemic cells. In vitro studies showed that CHD7 interacted with CBFb-SMMHC through RUNX1 and that CHD7 enhanced transcriptional activity of RUNX1 and CBFb-SMMHC on Csf1r, a RUNX1 target gene. Moreover, RNA sequencing of c-Kit1 cells showed that CHD7 functions mostly through altering the expression of RUNX1 target genes. Most importantly, Chd7 deficiency delayed Cbfb-MYH11– induced leukemia in both primary and transplanted mice. These data indicate that Chd7 is important for Cbfb-MYH11– induced leukemogenesis by facilitating RUNX1 regulation of transcription and cellular proliferation.

Original languageEnglish (US)
Pages (from-to)2431-2442
Number of pages12
Issue number22
StatePublished - Nov 30 2017

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology


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