Dependence on Myb expression is attenuated in myeloid leukaemia with N-terminal CEBPA mutations

Life Sci Alliance. 2019 Mar 15;2(2):e201800207. doi: 10.26508/lsa.201800207. Print 2019 Apr.


Mutations at the N- or C-terminus of C/EBPα are frequent in acute myeloid leukaemia (AML) with normal karyotype. Here, we investigate the role of the transcription factor Myb in AMLs driven by different combinations of CEBPA mutations. Using knockdown of Myb in murine cell lines modelling the spectrum of CEBPA mutations, we show that the effect of reduced Myb depends on the mutational status of the two Cebpa alleles. Importantly, Myb knockdown fails to override the block in myeloid differentiation in cells with biallelic N-terminal C/EBPα mutations, demonstrating for the first time that the dependency on Myb is much lower in AML with this mutational profile. By comparing gene expression following Myb knockdown and chromatin immunoprecipitation sequencing data for the binding of C/EBPα isoforms, we provide evidence for a functional cooperation between C/EBPα and Myb in the maintenance of AML. This co-dependency breaks down when both alleles of CEBPA harbour N-terminal mutations, as a subset of C/EBPα-regulated genes only bind the short p30 C/EBPα isoform and, unlike other C/EBPα-regulated genes, do so without a requirement for Myb.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Apoptosis / genetics
  • CCAAT-Enhancer-Binding Proteins / genetics*
  • Cell Differentiation / genetics
  • Cell Line, Tumor
  • Cell Survival / genetics
  • Gene Expression Regulation, Neoplastic
  • Gene Knockdown Techniques
  • Leukemia, Myeloid, Acute / genetics*
  • Leukemia, Myeloid, Acute / pathology*
  • Mice
  • Mutation / genetics*
  • Phenotype
  • Protein Isoforms / genetics
  • Proto-Oncogene Proteins c-myb / genetics*
  • RNA, Small Interfering / genetics
  • Transfection


  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, mouse
  • Protein Isoforms
  • Proto-Oncogene Proteins c-myb
  • RNA, Small Interfering