Cohesin-dependent regulation of gene expression during differentiation is lost in cohesin-mutated myeloid malignancies

Blood. 2019 Dec 12;134(24):2195-2208. doi: 10.1182/blood.2019001553.

Abstract

Cohesin complex disruption alters gene expression, and cohesin mutations are common in myeloid neoplasia, suggesting a critical role in hematopoiesis. Here, we explore cohesin dynamics and regulation of hematopoietic stem cell homeostasis and differentiation. Cohesin binding increases at active regulatory elements only during erythroid differentiation. Prior binding of the repressive Ets transcription factor Etv6 predicts cohesin binding at these elements and Etv6 interacts with cohesin at chromatin. Depletion of cohesin severely impairs erythroid differentiation, particularly at Etv6-prebound loci, but augments self-renewal programs. Together with corroborative findings in acute myeloid leukemia and myelodysplastic syndrome patient samples, these data suggest cohesin-mediated alleviation of Etv6 repression is required for dynamic expression at critical erythroid genes during differentiation and how this may be perturbed in myeloid malignancies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism*
  • Cell Line, Tumor
  • Chromosomal Proteins, Non-Histone / genetics*
  • Chromosomal Proteins, Non-Histone / metabolism*
  • Cohesins
  • ETS Translocation Variant 6 Protein
  • Female
  • Gene Dosage
  • Gene Expression Regulation, Leukemic*
  • Hematopoietic Stem Cells / metabolism
  • Hematopoietic Stem Cells / pathology
  • Histones / metabolism
  • Humans
  • Male
  • Mutation*
  • Myeloproliferative Disorders / diagnosis
  • Myeloproliferative Disorders / genetics*
  • Myeloproliferative Disorders / metabolism*
  • Neoplasm Grading
  • Protein Binding
  • Proto-Oncogene Proteins c-ets / metabolism
  • Regulatory Sequences, Nucleic Acid
  • Repressor Proteins / metabolism

Substances

  • Biomarkers, Tumor
  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • Histones
  • Proto-Oncogene Proteins c-ets
  • Repressor Proteins