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A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1
PU.1 is a hematopoietic transcription factor that is required for the development of myeloid and B cells. PU.1 is also expressed in erythroid progenitors, where it blocks erythroid differentiation by binding to and inhibiting the main erythroid promoting factor, GATA-1. However, other mechanisms by...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111485/ https://www.ncbi.nlm.nih.gov/pubmed/21695229 http://dx.doi.org/10.1371/journal.pgen.1001392 |
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author | Wontakal, Sandeep N. Guo, Xingyi Will, Britta Shi, Minyi Raha, Debasish Mahajan, Milind C. Weissman, Sherman Snyder, Michael Steidl, Ulrich Zheng, Deyou Skoultchi, Arthur I. |
author_facet | Wontakal, Sandeep N. Guo, Xingyi Will, Britta Shi, Minyi Raha, Debasish Mahajan, Milind C. Weissman, Sherman Snyder, Michael Steidl, Ulrich Zheng, Deyou Skoultchi, Arthur I. |
author_sort | Wontakal, Sandeep N. |
collection | PubMed |
description | PU.1 is a hematopoietic transcription factor that is required for the development of myeloid and B cells. PU.1 is also expressed in erythroid progenitors, where it blocks erythroid differentiation by binding to and inhibiting the main erythroid promoting factor, GATA-1. However, other mechanisms by which PU.1 affects the fate of erythroid progenitors have not been thoroughly explored. Here, we used ChIP-Seq analysis for PU.1 and gene expression profiling in erythroid cells to show that PU.1 regulates an extensive network of genes that constitute major pathways for controlling growth and survival of immature erythroid cells. By analyzing fetal liver erythroid progenitors from mice with low PU.1 expression, we also show that the earliest erythroid committed cells are dramatically reduced in vivo. Furthermore, we find that PU.1 also regulates many of the same genes and pathways in other blood cells, leading us to propose that PU.1 is a multifaceted factor with overlapping, as well as distinct, functions in several hematopoietic lineages. |
format | Online Article Text |
id | pubmed-3111485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31114852011-06-21 A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 Wontakal, Sandeep N. Guo, Xingyi Will, Britta Shi, Minyi Raha, Debasish Mahajan, Milind C. Weissman, Sherman Snyder, Michael Steidl, Ulrich Zheng, Deyou Skoultchi, Arthur I. PLoS Genet Research Article PU.1 is a hematopoietic transcription factor that is required for the development of myeloid and B cells. PU.1 is also expressed in erythroid progenitors, where it blocks erythroid differentiation by binding to and inhibiting the main erythroid promoting factor, GATA-1. However, other mechanisms by which PU.1 affects the fate of erythroid progenitors have not been thoroughly explored. Here, we used ChIP-Seq analysis for PU.1 and gene expression profiling in erythroid cells to show that PU.1 regulates an extensive network of genes that constitute major pathways for controlling growth and survival of immature erythroid cells. By analyzing fetal liver erythroid progenitors from mice with low PU.1 expression, we also show that the earliest erythroid committed cells are dramatically reduced in vivo. Furthermore, we find that PU.1 also regulates many of the same genes and pathways in other blood cells, leading us to propose that PU.1 is a multifaceted factor with overlapping, as well as distinct, functions in several hematopoietic lineages. Public Library of Science 2011-06-09 /pmc/articles/PMC3111485/ /pubmed/21695229 http://dx.doi.org/10.1371/journal.pgen.1001392 Text en Wontakal et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wontakal, Sandeep N. Guo, Xingyi Will, Britta Shi, Minyi Raha, Debasish Mahajan, Milind C. Weissman, Sherman Snyder, Michael Steidl, Ulrich Zheng, Deyou Skoultchi, Arthur I. A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 |
title | A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 |
title_full | A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 |
title_fullStr | A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 |
title_full_unstemmed | A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 |
title_short | A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 |
title_sort | large gene network in immature erythroid cells is controlled by the myeloid and b cell transcriptional regulator pu.1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111485/ https://www.ncbi.nlm.nih.gov/pubmed/21695229 http://dx.doi.org/10.1371/journal.pgen.1001392 |
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