Selective Expression of mRNA Coding for the Truncated Form of Erythropoietin Receptor in Hematopoietic Cells and Its Decrease in Patients With Polycythemia Vera

Author:

Chiba Shigeru1,Takahashi Tokiharu1,Takeshita Kenichi1,Minowada Jun1,Yazaki Yoshio1,Ruddle Frank H.1,Hirai Hisamaru1

Affiliation:

1. From the Third Department of Internal Medicine and Department of Cell Therapy and Transplantation Medicine, Faculty of Medicine, University of Tokyo, Tokyo Japan; Departments of Biology, Human Genetics, and Medicine, Yale University, New Haven, CT; Division of Hematology, Department of Internal Medicine, New York University Medical Center, New York, NY; and Fujisaki Cell Center, Hayashibara Biochemical Research Laboratories, Okayama, Japan.

Abstract

The mRNA encoding full-length erythropoietin (EPO) receptor (EPOR-F ) comprises exons I through VIII. Another membrane-bound EPOR (EPOR-T) isoform has a truncated cytoplasmic region and is encoded by the mRNA containing unspliced intron VII (EPOR-T mRNA). EPOR-T is believed to have a dominantly negative function against EPOR-F. We show that EPOR-T mRNA is markedly decreased in the blood cells of patients with polycythemia vera (PV). We also show that EPOR-T mRNA is not detected in erythroid/megakaryocytic leukemia cell lines, but is expressed in nonerythroid/nonmegakaryocytic lines, suggesting the presence of a cell type–specific system by which intron VII of the EPOR transcript is spliced. Deregulation of this splicing system in early hematopoietic progenitors possibly explains the profound decrease in EPOR-T mRNA and consequent pathophysiology of PV.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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