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Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes
Transcription factor-induced lineage reprogramming or transdifferentiation experiments are essential for understanding the plasticity of differentiated cells. These experiments helped to define the specific role of transcription factors in conferring cell identity and played a key role in the develo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299990/ https://www.ncbi.nlm.nih.gov/pubmed/22086955 http://dx.doi.org/10.1093/nar/gkr1015 |
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author | Rodríguez-Ubreva, Javier Ciudad, Laura Gómez-Cabrero, David Parra, Maribel Bussmann, Lars H. di Tullio, Alessandro Kallin, Eric M. Tegnér, Jesper Graf, Thomas Ballestar, Esteban |
author_facet | Rodríguez-Ubreva, Javier Ciudad, Laura Gómez-Cabrero, David Parra, Maribel Bussmann, Lars H. di Tullio, Alessandro Kallin, Eric M. Tegnér, Jesper Graf, Thomas Ballestar, Esteban |
author_sort | Rodríguez-Ubreva, Javier |
collection | PubMed |
description | Transcription factor-induced lineage reprogramming or transdifferentiation experiments are essential for understanding the plasticity of differentiated cells. These experiments helped to define the specific role of transcription factors in conferring cell identity and played a key role in the development of the regenerative medicine field. We here investigated the acquisition of DNA methylation changes during C/EBPα-induced pre-B cell to macrophage transdifferentiation. Unexpectedly, cell lineage conversion occurred without significant changes in DNA methylation not only in key B cell- and macrophage-specific genes but also throughout the entire set of genes differentially methylated between the two parental cell types. In contrast, active and repressive histone modification marks changed according to the expression levels of these genes. We also demonstrated that C/EBPα and RNA Pol II are associated with the methylated promoters of macrophage-specific genes in reprogrammed macrophages without inducing methylation changes. Our findings not only provide insights about the extent and hierarchy of epigenetic events in pre-B cell to macrophage transdifferentiation but also show an important difference to reprogramming towards pluripotency where promoter DNA demethylation plays a pivotal role. |
format | Online Article Text |
id | pubmed-3299990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32999902012-03-13 Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes Rodríguez-Ubreva, Javier Ciudad, Laura Gómez-Cabrero, David Parra, Maribel Bussmann, Lars H. di Tullio, Alessandro Kallin, Eric M. Tegnér, Jesper Graf, Thomas Ballestar, Esteban Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Transcription factor-induced lineage reprogramming or transdifferentiation experiments are essential for understanding the plasticity of differentiated cells. These experiments helped to define the specific role of transcription factors in conferring cell identity and played a key role in the development of the regenerative medicine field. We here investigated the acquisition of DNA methylation changes during C/EBPα-induced pre-B cell to macrophage transdifferentiation. Unexpectedly, cell lineage conversion occurred without significant changes in DNA methylation not only in key B cell- and macrophage-specific genes but also throughout the entire set of genes differentially methylated between the two parental cell types. In contrast, active and repressive histone modification marks changed according to the expression levels of these genes. We also demonstrated that C/EBPα and RNA Pol II are associated with the methylated promoters of macrophage-specific genes in reprogrammed macrophages without inducing methylation changes. Our findings not only provide insights about the extent and hierarchy of epigenetic events in pre-B cell to macrophage transdifferentiation but also show an important difference to reprogramming towards pluripotency where promoter DNA demethylation plays a pivotal role. Oxford University Press 2012-03 2011-11-15 /pmc/articles/PMC3299990/ /pubmed/22086955 http://dx.doi.org/10.1093/nar/gkr1015 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Rodríguez-Ubreva, Javier Ciudad, Laura Gómez-Cabrero, David Parra, Maribel Bussmann, Lars H. di Tullio, Alessandro Kallin, Eric M. Tegnér, Jesper Graf, Thomas Ballestar, Esteban Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes |
title | Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes |
title_full | Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes |
title_fullStr | Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes |
title_full_unstemmed | Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes |
title_short | Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes |
title_sort | pre-b cell to macrophage transdifferentiation without significant promoter dna methylation changes |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299990/ https://www.ncbi.nlm.nih.gov/pubmed/22086955 http://dx.doi.org/10.1093/nar/gkr1015 |
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