The DEK Oncoprotein Is a Critical Component of the EKLF/KLF1 Enhancer in Erythroid Cells

Author:

Lohmann Felix1,Dangeti Mohan1,Soni Shefali1,Chen Xiaoyong1,Planutis Antanas1,Baron Margaret H.1234,Choi Kyunghee5,Bieker James J.123

Affiliation:

1. Department of Developmental and Regenerative Biology, Mount Sinai School of Medicine, New York, New York, USA

2. Black Family Stem Cell Institute, Mount Sinai School of Medicine, New York, New York, USA

3. Tisch Cancer Institute, Mount Sinai School of Medicine, New York, New York, USA

4. Department of Medicine, Mount Sinai School of Medicine, New York, New York, USA

5. Department of Pathology, Washington University School of Medicine, St. Louis, Missouri, USA

Abstract

ABSTRACT Understanding how transcriptional regulators are themselves controlled is important in attaining a complete picture of the intracellular effects that follow signaling cascades during early development and cell-restricted differentiation. We have addressed this issue by focusing on the regulation of EKLF/KLF1, a zinc finger transcription factor that plays a necessary role in the global regulation of erythroid gene expression. Using biochemical affinity purification, we have identified the DEK oncoprotein as a critical factor that interacts with an essential upstream enhancer element of the EKLF promoter and exerts a positive effect on EKLF levels. This element also binds a core set of erythroid transcription factors, suggesting that DEK is part of a tissue-restricted enhanceosome that contains BMP4-dependent and -independent components. Together with local enrichment of properly coded histones and an open chromatin domain, optimal transcriptional activation of the EKLF locus can be established.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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