An autonomous CEBPA enhancer specific for myeloid-lineage priming and neutrophilic differentiation

Author:

Avellino Roberto1,Havermans Marije1,Erpelinck Claudia1,Sanders Mathijs A.1,Hoogenboezem Remco1,van de Werken Harmen J. G.234ORCID,Rombouts Elwin1,van Lom Kirsten1,van Strien Paulina M. H.1,Gebhard Claudia56,Rehli Michael56,Pimanda John7,Beck Dominik7,Erkeland Stefan18,Kuiken Thijs9,de Looper Hans1,Gröschel Stefan110,Touw Ivo1,Bindels Eric1,Delwel Ruud1

Affiliation:

1. Department of Hematology,

2. Cancer Computational Biology Center,

3. Department of Cell Biology, and

4. Department of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands;

5. Department of Internal Medicine III and

6. Regensburg Centre for Interventional Immunology, University Hospital Regensburg, Regensburg, Germany;

7. Prince of Wales Clinical Schools and Lowy Cancer Research Centre, The University of New South Wales, Sydney, NSW, Australia;

8. Department of Immunology and

9. Department of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands; and

10. Department of Translational Oncology, National Center for Tumor Diseases, Deutsches Krebsforschungszentrum (DKFZ), Heidelberg, Germany

Abstract

Key Points The CEBPA locus harbors 14 enhancers of which distinct combinations are active in different CEBPA-expressing tissues. A +42-kb enhancer is required for myeloid-lineage priming to drive adequate CEBPA expression levels necessary for neutrophilic maturation.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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