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

Blood. 2019 Dec 12;134(24):2195-2208
Daniel Sasca 1 , Haiyang Yun 2 , George Giotopoulos 2 , Jakub Szybinski 1 , Theo Evan 2 , Nicola K Wilson 2 , Moritz Gerstung 3 , Paolo Gallipoli 2 , Anthony R Green 2 , Robert Hills 4 , Nigel Russell 5 , Cameron S Osborne 6 , Elli Papaemmanuil 7 , Berthold Göttgens 2 , Peter Campbell 8 , Brian J P Huntly 2
Daniel Sasca 1 , Haiyang Yun 2 , George Giotopoulos 2 , Jakub Szybinski 1 , Theo Evan 2 , Nicola K Wilson 2 , Moritz Gerstung 3 , Paolo Gallipoli 2 , Anthony R Green 2 , Robert Hills 4 , Nigel Russell 5 , Cameron S Osborne 6 , Elli Papaemmanuil 7 , Berthold Göttgens 2 , Peter Campbell 8 , Brian J P Huntly 2
+ et al

[No authors listed]

Author information
  • 1 Department of Hematology, Oncology and Pneumology, University Medical Center Mainz, Mainz, Germany.
  • 2 Department of Haematology, University of Cambridge, Cambridge, United Kingdom.
  • 3 European Bioinformatic Institute, Genome Campus, Hinxton, United Kingdom.
  • 4 Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
  • 5 Department of Haematology, University of Nottingham, Nottingham, United Kingdom.
  • 6 Department of Medical and Molecular Genetics, Kings College London, United Kingdom.
  • 7 Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY; and.
  • 8 Cancer, Ageing and Somatic Mutation Programme, Wellcome Trust Sanger Institute, Genome Campus, Hinxton, United Kingdom.

摘要


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.