Secondary Logo

Institutional members access full text with Ovid®

Share this article on:

Integrative view on how erythropoietin signaling controls transcription patterns in erythroid cells

Perreault, Andrea, A.a; Venters, Bryan, J.a,b,c

Current Opinion in Hematology: May 2018 - Volume 25 - Issue 3 - p 189–195
doi: 10.1097/MOH.0000000000000415
ERYTHROID SYSTEM AND ITS DISEASES: Edited by Narla Mohandas

Purpose of review Erythropoietin (EPO) is necessary and sufficient to trigger dynamic transcriptional patterns that drive the differentiation of erythroid precursor cells into mature, enucleated red cells. Because the molecular cloning and Food and Drug Administration approval for the therapeutic use of EPO over 30 years ago, a detailed understanding of how EPO works has advanced substantially. Yet, the precise epigenetic and transcriptional mechanisms by which EPO signaling controls erythroid expression patterns remains poorly understood. This review focuses on the current state of erythroid biology in regards to EPO signaling from human genetics and functional genomics perspectives.

Recent findings The goal of this review is to provide an integrative view of the gene regulatory underpinnings for erythroid expression patterns that are dynamically shaped during erythroid differentiation. Here, we highlight vignettes connecting recent insights into a genome-wide association study linking an EPO mutation to anemia, a study linking EPO-signaling to signal transducer and activator of transcription 5 (STAT5) chromatin occupancy and enhancers, and studies that examine the molecular mechanisms driving topological chromatin organization in erythroid cells.

Summary The genetic, epigenetic, and gene regulatory mechanisms underlying how hormone signal transduction influences erythroid gene expression remains only partly understood. A detailed understanding of these molecular pathways and how they intersect with one another will provide the basis for novel strategies to treat anemia and potentially other hematological diseases. As new regulators and signal transducers of EPO-signaling continue to emerge, new clinically relevant targets may be identified that improve the specificity and effectiveness of EPO therapy.

aChemical and Physical Biology Program and Department of Molecular Physiology and Biophysics at Vanderbilt University

bVanderbilt Genetics Institute

cVanderbilt Ingram Cancer Center at Vanderbilt University, Nashville, Tennessee, USA

Correspondence to Bryan J. Venters, 2215 Garland Ave., Nashville, TN 37232, USA. Tel: +615 322 4761; e-mail: bryan.venters@vanderbilt.edu

Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.