Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.

Patients with mutations of the THRA gene exhibit classical features of hypothyroidism, including erythroid disorders. We previously created a mutant mouse expressing a mutated TRα1 (denoted as PV; Thra1PV/+ mouse) that faithfully reproduces the classical hypothyroidism seen in patients. Using Thra1P...

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Main Authors: Sunmi Park, Cho Rong Han, Jeong Won Park, Li Zhao, Xuguang Zhu, Mark Willingham, David M Bodine, Sheue-Yann Cheng
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-09-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006991&type=printable
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author Sunmi Park
Cho Rong Han
Jeong Won Park
Li Zhao
Xuguang Zhu
Mark Willingham
David M Bodine
Sheue-Yann Cheng
author_facet Sunmi Park
Cho Rong Han
Jeong Won Park
Li Zhao
Xuguang Zhu
Mark Willingham
David M Bodine
Sheue-Yann Cheng
author_sort Sunmi Park
collection DOAJ
description Patients with mutations of the THRA gene exhibit classical features of hypothyroidism, including erythroid disorders. We previously created a mutant mouse expressing a mutated TRα1 (denoted as PV; Thra1PV/+ mouse) that faithfully reproduces the classical hypothyroidism seen in patients. Using Thra1PV/+ mice, we explored how the TRα1PV mutant acted to cause abnormalities in erythropoiesis. Thra1PV/+ mice exhibited abnormal red blood cell indices similarly as reported for patients. The total bone marrow cells and erythrocytic progenitors were markedly reduced in the bone marrow of Thra1PV/+ mice. In vitro terminal differentiation assays showed a significant reduction of mature erythrocytes in Thra1PV/+ mice. In wild-type mice, the clonogenic potential of progenitors in the erythrocytic lineage was stimulated by thyroid hormone (T3), suggesting that T3 could directly accelerate the differentiation of progenitors to mature erythrocytes. Analysis of gene expression profiles showed that the key regulator of erythropoiesis, the Gata-1 gene, and its regulated genes, such as the Klf1, β-globin, dematin genes, CAII, band3 and eALAS genes, involved in the maturation of erythrocytes, was decreased in the bone marrow cells of Thra1PV/+ mice. We further elucidated that the Gata-1 gene was a T3-directly regulated gene and that TRα1PV could impair erythropoiesis via repression of the Gata-1 gene and its regulated genes. These results provide new insights into how TRα1 mutants acted to cause erythroid abnormalities in patients with mutations of the THRA gene. Importantly, the Thra1PV/+ mouse could serve as a preclinical mouse model to identify novel molecular targets for treatment of erythroid disorders.
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spelling doaj-art-d4f2878eafa2414cbdb331d679ab8c0d2025-08-20T02:03:47ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042017-09-01139e100699110.1371/journal.pgen.1006991Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.Sunmi ParkCho Rong HanJeong Won ParkLi ZhaoXuguang ZhuMark WillinghamDavid M BodineSheue-Yann ChengPatients with mutations of the THRA gene exhibit classical features of hypothyroidism, including erythroid disorders. We previously created a mutant mouse expressing a mutated TRα1 (denoted as PV; Thra1PV/+ mouse) that faithfully reproduces the classical hypothyroidism seen in patients. Using Thra1PV/+ mice, we explored how the TRα1PV mutant acted to cause abnormalities in erythropoiesis. Thra1PV/+ mice exhibited abnormal red blood cell indices similarly as reported for patients. The total bone marrow cells and erythrocytic progenitors were markedly reduced in the bone marrow of Thra1PV/+ mice. In vitro terminal differentiation assays showed a significant reduction of mature erythrocytes in Thra1PV/+ mice. In wild-type mice, the clonogenic potential of progenitors in the erythrocytic lineage was stimulated by thyroid hormone (T3), suggesting that T3 could directly accelerate the differentiation of progenitors to mature erythrocytes. Analysis of gene expression profiles showed that the key regulator of erythropoiesis, the Gata-1 gene, and its regulated genes, such as the Klf1, β-globin, dematin genes, CAII, band3 and eALAS genes, involved in the maturation of erythrocytes, was decreased in the bone marrow cells of Thra1PV/+ mice. We further elucidated that the Gata-1 gene was a T3-directly regulated gene and that TRα1PV could impair erythropoiesis via repression of the Gata-1 gene and its regulated genes. These results provide new insights into how TRα1 mutants acted to cause erythroid abnormalities in patients with mutations of the THRA gene. Importantly, the Thra1PV/+ mouse could serve as a preclinical mouse model to identify novel molecular targets for treatment of erythroid disorders.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006991&type=printable
spellingShingle Sunmi Park
Cho Rong Han
Jeong Won Park
Li Zhao
Xuguang Zhu
Mark Willingham
David M Bodine
Sheue-Yann Cheng
Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.
PLoS Genetics
title Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.
title_full Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.
title_fullStr Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.
title_full_unstemmed Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.
title_short Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.
title_sort defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006991&type=printable
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