HERF1, a Novel Hematopoiesis-Specific RING Finger Protein, Is Required for Terminal Differentiation of Erythroid Cells

Author:

Harada Hironori1,Harada Yuka1,O’Brien Darin P.1,Rice Dennis S.2,Naeve Clayton W.3,Downing James R.145

Affiliation:

1. Departments of Pathology and Laboratory Medicine,1

2. Developmental Neurobiology, 2 and

3. Center for Biotechnology, 3 St. Jude Children’s Research Hospital, and

4. Tumor Cell Biology 4 and

5. Department of Pathology, University of Tennessee College of Medicine, 5 Memphis, Tennessee

Abstract

ABSTRACT The AML1/core binding factor β (CBFβ) transcription factor is essential for definitive hematopoiesis; however, the downstream pathways through which it functions remain incompletely defined. Using a differential cloning approach to define components of this pathway, we have identified a novel gene designated HERF1 (for hematopoietic RING finger 1), whose expression during development is dependent on the presence of functional AML1/CBFβ. HERF1 contains a tripartite RING finger–B box–α-helical coiled-coil domain and a C-terminal region homologous to the ret proto-oncogene-encoded finger protein. Expression of HERF1 during embryogenesis coincides with the appearance of definitive erythropoiesis and in adult mice is restricted to erythroid cells, increasing 30-fold during terminal differentiation. Importantly, inhibition of HERF1 expression blocked terminal erythroid differentiation of the murine erythroleukemia cell line MEL, whereas its overexpression induced erythroid maturation. These results suggest an important role for this protein in erythropoiesis.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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