Defining the functionally sufficient regulatory region and liver-specific roles of the erythropoietin gene by transgene complementation

• Published in: Life sciences (1973) 2021-03, Vol.269, p.119075-119075, Article 119075
• Main Authors: Yamazaki, Shun, Hirano, Ikuo, Kato, Koichiro, Yamamoto, Masayuki, Suzuki, Norio
• Format: Article
• Language: English
• Subjects: Anemia; Anemia - genetics; Anemia - pathology; Anemia - prevention & control; Animals; Complementation; Defects; Embryos; Erythroid cells; Erythropoiesis; Erythropoietin; Erythropoietin - genetics; Erythropoietin - metabolism; Gene regulation; Growth factors; Hypoxia; Kidneys; Liver; Liver - metabolism; Mice; Mice, Knockout; Mice, Transgenic; Neonates; Organs; Recombination; Regulatory mechanisms (biology); Regulatory Sequences, Nucleic Acid; Spleen; Transcription; Transgenes; Transgenes - physiology; Transgenic mouse
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2021.119075

Erythropoietin (EPO) is an essential growth factor for erythroid cells and is mainly secreted from the kidneys and subsidiarily from the livers of adult mammals in an anemia/hypoxia-inducible manner. To elucidate the regulatory mechanisms of stress-inducible and cell type-specific Epo gene transcription, the rate-limiting step of EPO production, we investigated the sufficiency of a 180-kb genomic fragment flanking the mouse Epo gene locus for recapitulating endogenous Epo gene function by a transgene complementation strategy. While Epo gene-deficient mice exhibited lethal anemia in utero with defects in erythroblast proliferation and maturation, Epo-knockout mice integrated with the 180-kb Epo transgene showed normal erythropoiesis throughout life. In the transgene-rescued mice, liver-specific deletion of the transgene by the Cre-loxP recombination system caused neonatal anemia with erythropoietic defects in the liver but not in the spleen, indicating the essential function of hepatic EPO on normal erythropoiesis in the liver, which is the major erythropoietic site in late embryonic and neonatal stages. These results demonstrate that the 180 kb Epo gene flanking region contains the fully functional Epo gene unit and that EPO from the liver dominantly stimulates hepatic erythropoiesis but contributes less to erythropoiesis in other organs. [Display omitted] •The 180-kb gene fragment flanking the Epo gene is functionally sufficient to regulate in vivo Epo gene expression.•The liver is the major erythropoietic organ in late embryonic and neonatal stages.•Hepatic erythropoiesis requires hepatic EPO production.