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Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate

Self-renewal and differentiation of hematopoietic stem cells (HSCs) are orchestrated by the combinatorial action of transcription factors and epigenetic regulators. Here, we have explored the mechanism by which histone H4 lysine 16 acetyltransferase MOF regulates erythropoiesis. Single-cell RNA sequ...

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Autores principales: Pessoa Rodrigues, Cecilia, Herman, Josip Stefan, Herquel, Benjamin, Valsecchi, Claudia Isabelle Keller, Stehle, Thomas, Grün, Dominic, Akhtar, Asifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314555/
https://www.ncbi.nlm.nih.gov/pubmed/32671208
http://dx.doi.org/10.1126/sciadv.aaz4815
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author Pessoa Rodrigues, Cecilia
Herman, Josip Stefan
Herquel, Benjamin
Valsecchi, Claudia Isabelle Keller
Stehle, Thomas
Grün, Dominic
Akhtar, Asifa
author_facet Pessoa Rodrigues, Cecilia
Herman, Josip Stefan
Herquel, Benjamin
Valsecchi, Claudia Isabelle Keller
Stehle, Thomas
Grün, Dominic
Akhtar, Asifa
author_sort Pessoa Rodrigues, Cecilia
collection PubMed
description Self-renewal and differentiation of hematopoietic stem cells (HSCs) are orchestrated by the combinatorial action of transcription factors and epigenetic regulators. Here, we have explored the mechanism by which histone H4 lysine 16 acetyltransferase MOF regulates erythropoiesis. Single-cell RNA sequencing and chromatin immunoprecipitation sequencing uncovered that MOF influences erythroid trajectory by dynamic recruitment to chromatin and its haploinsufficiency causes accumulation of a transient HSC population. A regulatory network consisting of MOF, RUNX1, and GFI1B is critical for erythroid fate commitment. GFI1B acts as a Mof activator which is necessary and sufficient for cell type-specific induction of Mof expression. Plasticity of Mof-depleted HSCs can be rescued by expression of a downstream effector, Gata1, or by rebalancing acetylation via a histone deacetylase inhibitor. Accurate timing and dosage of Mof expression act as a rheostat for the feedforward transcription factor network that safeguards progression along the erythroid fate.
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spelling pubmed-73145552020-07-14 Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate Pessoa Rodrigues, Cecilia Herman, Josip Stefan Herquel, Benjamin Valsecchi, Claudia Isabelle Keller Stehle, Thomas Grün, Dominic Akhtar, Asifa Sci Adv Research Articles Self-renewal and differentiation of hematopoietic stem cells (HSCs) are orchestrated by the combinatorial action of transcription factors and epigenetic regulators. Here, we have explored the mechanism by which histone H4 lysine 16 acetyltransferase MOF regulates erythropoiesis. Single-cell RNA sequencing and chromatin immunoprecipitation sequencing uncovered that MOF influences erythroid trajectory by dynamic recruitment to chromatin and its haploinsufficiency causes accumulation of a transient HSC population. A regulatory network consisting of MOF, RUNX1, and GFI1B is critical for erythroid fate commitment. GFI1B acts as a Mof activator which is necessary and sufficient for cell type-specific induction of Mof expression. Plasticity of Mof-depleted HSCs can be rescued by expression of a downstream effector, Gata1, or by rebalancing acetylation via a histone deacetylase inhibitor. Accurate timing and dosage of Mof expression act as a rheostat for the feedforward transcription factor network that safeguards progression along the erythroid fate. American Association for the Advancement of Science 2020-05-20 /pmc/articles/PMC7314555/ /pubmed/32671208 http://dx.doi.org/10.1126/sciadv.aaz4815 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Pessoa Rodrigues, Cecilia
Herman, Josip Stefan
Herquel, Benjamin
Valsecchi, Claudia Isabelle Keller
Stehle, Thomas
Grün, Dominic
Akhtar, Asifa
Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate
title Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate
title_full Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate
title_fullStr Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate
title_full_unstemmed Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate
title_short Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate
title_sort temporal expression of mof acetyltransferase primes transcription factor networks for erythroid fate
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314555/
https://www.ncbi.nlm.nih.gov/pubmed/32671208
http://dx.doi.org/10.1126/sciadv.aaz4815
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