SATB1 Chromatin Loops Regulate Megakaryocyte/Erythroid Progenitor Expansion by Facilitating HSP70 and GATA1 Induction

Author:

Wilkes Mark C1ORCID,Chae Hee-Don1,Scanlon Vanessa2,Cepika Alma-Martina3,Wentworth Ethan P1,Saxena Mallika1,Eskin Ascia4,Chen Zugen4,Glader Bert1,Grazia Roncarolo Maria3,Nelson Stanley F4,Sakamoto Kathleen M1

Affiliation:

1. Division of Hematology/Oncology, Department of Pediatrics, Stanford University , Stanford, CA , USA

2. Department of Laboratory Medicine, Yale Stem Cell Center, Yale Cooperative Center of Excellence in Hematology, Yale School of Medicine , New Haven, CT , USA

3. Institute for Stem Cell Biology and Regenerative Medicine, Department of Genetics, Stanford University School of Medicine , Stanford, CA , USA

4. Department of Pathology and Laboratory Medicine¸ David Geffen School of Medicine, University of California , Los Angeles, CA , USA

Abstract

Abstract Diamond Blackfan anemia (DBA) is an inherited bone marrow failure syndrome associated with severe anemia, congenital malformations, and an increased risk of developing cancer. The chromatin-binding special AT-rich sequence-binding protein-1 (SATB1) is downregulated in megakaryocyte/erythroid progenitors (MEPs) in patients and cell models of DBA, leading to a reduction in MEP expansion. Here we demonstrate that SATB1 expression is required for the upregulation of the critical erythroid factors heat shock protein 70 (HSP70) and GATA1 which accompanies MEP differentiation. SATB1 binding to specific sites surrounding the HSP70 genes promotes chromatin loops that are required for the induction of HSP70, which, in turn, promotes GATA1 induction. This demonstrates that SATB1, although gradually downregulated during myelopoiesis, maintains a biological function in early myeloid progenitors.

Funder

National Institutes of Health

Maternal Child Health Research Institute fellowship

Department of Defense

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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