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Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation
Here, we describe that lysine-specific demethylase 1 (Lsd1/KDM1a), which demethylates histone H3 on Lys4 or Lys9 (H3K4/K9), is an indispensible epigenetic governor of hematopoietic differentiation. Integrative genomic analysis, combining global occupancy of Lsd1, genome-wide analysis of its substrat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687337/ https://www.ncbi.nlm.nih.gov/pubmed/23795291 http://dx.doi.org/10.7554/eLife.00633 |
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author | Kerenyi, Marc A Shao, Zhen Hsu, Yu-Jung Guo, Guoji Luc, Sidinh O'Brien, Kassandra Fujiwara, Yuko Peng, Cong Nguyen, Minh Orkin, Stuart H |
author_facet | Kerenyi, Marc A Shao, Zhen Hsu, Yu-Jung Guo, Guoji Luc, Sidinh O'Brien, Kassandra Fujiwara, Yuko Peng, Cong Nguyen, Minh Orkin, Stuart H |
author_sort | Kerenyi, Marc A |
collection | PubMed |
description | Here, we describe that lysine-specific demethylase 1 (Lsd1/KDM1a), which demethylates histone H3 on Lys4 or Lys9 (H3K4/K9), is an indispensible epigenetic governor of hematopoietic differentiation. Integrative genomic analysis, combining global occupancy of Lsd1, genome-wide analysis of its substrates H3K4 monomethylation and dimethylation, and gene expression profiling, reveals that Lsd1 represses hematopoietic stem and progenitor cell (HSPC) gene expression programs during hematopoietic differentiation. We found that Lsd1 acts at transcription start sites, as well as enhancer regions. Loss of Lsd1 was associated with increased H3K4me1 and H3K4me2 methylation on HSPC genes and gene derepression. Failure to fully silence HSPC genes compromised differentiation of hematopoietic stem cells as well as mature blood cell lineages. Collectively, our data indicate that Lsd1-mediated concurrent repression of enhancer and promoter activity of stem and progenitor cell genes is a pivotal epigenetic mechanism required for proper hematopoietic maturation. DOI: http://dx.doi.org/10.7554/eLife.00633.001 |
format | Online Article Text |
id | pubmed-3687337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36873372013-06-21 Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation Kerenyi, Marc A Shao, Zhen Hsu, Yu-Jung Guo, Guoji Luc, Sidinh O'Brien, Kassandra Fujiwara, Yuko Peng, Cong Nguyen, Minh Orkin, Stuart H eLife Developmental Biology and Stem Cells Here, we describe that lysine-specific demethylase 1 (Lsd1/KDM1a), which demethylates histone H3 on Lys4 or Lys9 (H3K4/K9), is an indispensible epigenetic governor of hematopoietic differentiation. Integrative genomic analysis, combining global occupancy of Lsd1, genome-wide analysis of its substrates H3K4 monomethylation and dimethylation, and gene expression profiling, reveals that Lsd1 represses hematopoietic stem and progenitor cell (HSPC) gene expression programs during hematopoietic differentiation. We found that Lsd1 acts at transcription start sites, as well as enhancer regions. Loss of Lsd1 was associated with increased H3K4me1 and H3K4me2 methylation on HSPC genes and gene derepression. Failure to fully silence HSPC genes compromised differentiation of hematopoietic stem cells as well as mature blood cell lineages. Collectively, our data indicate that Lsd1-mediated concurrent repression of enhancer and promoter activity of stem and progenitor cell genes is a pivotal epigenetic mechanism required for proper hematopoietic maturation. DOI: http://dx.doi.org/10.7554/eLife.00633.001 eLife Sciences Publications, Ltd 2013-06-18 /pmc/articles/PMC3687337/ /pubmed/23795291 http://dx.doi.org/10.7554/eLife.00633 Text en Copyright © 2013, Kerenyi et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Kerenyi, Marc A Shao, Zhen Hsu, Yu-Jung Guo, Guoji Luc, Sidinh O'Brien, Kassandra Fujiwara, Yuko Peng, Cong Nguyen, Minh Orkin, Stuart H Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
title | Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
title_full | Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
title_fullStr | Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
title_full_unstemmed | Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
title_short | Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
title_sort | histone demethylase lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687337/ https://www.ncbi.nlm.nih.gov/pubmed/23795291 http://dx.doi.org/10.7554/eLife.00633 |
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