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Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties
High-mobility group A (HMGA) proteins have been examined to understand their participation as structural epigenetic chromatin factors that confer stem-like properties to embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs), and cancer stem cells (CSCs). The function of HMGA was evalua...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941823/ https://www.ncbi.nlm.nih.gov/pubmed/29853899 http://dx.doi.org/10.1155/2018/3698078 |
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author | Giancotti, Vincenzo Bergamin, Natascha Cataldi, Palmina Rizzi, Claudio |
author_facet | Giancotti, Vincenzo Bergamin, Natascha Cataldi, Palmina Rizzi, Claudio |
author_sort | Giancotti, Vincenzo |
collection | PubMed |
description | High-mobility group A (HMGA) proteins have been examined to understand their participation as structural epigenetic chromatin factors that confer stem-like properties to embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs), and cancer stem cells (CSCs). The function of HMGA was evaluated in conjunction with that of other epigenetic factors such as histones and microRNAs (miRs), taking into consideration the posttranscriptional modifications (PTMs) of histones (acetylation and methylation) and DNA methylation. HMGA proteins were coordinated or associated with histone and DNA modification and the expression of the factors related to pluripotency. CSCs showed remarkable differences compared with ESCs and iPSCs. |
format | Online Article Text |
id | pubmed-5941823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-59418232018-05-31 Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties Giancotti, Vincenzo Bergamin, Natascha Cataldi, Palmina Rizzi, Claudio Int J Cell Biol Review Article High-mobility group A (HMGA) proteins have been examined to understand their participation as structural epigenetic chromatin factors that confer stem-like properties to embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs), and cancer stem cells (CSCs). The function of HMGA was evaluated in conjunction with that of other epigenetic factors such as histones and microRNAs (miRs), taking into consideration the posttranscriptional modifications (PTMs) of histones (acetylation and methylation) and DNA methylation. HMGA proteins were coordinated or associated with histone and DNA modification and the expression of the factors related to pluripotency. CSCs showed remarkable differences compared with ESCs and iPSCs. Hindawi 2018-04-24 /pmc/articles/PMC5941823/ /pubmed/29853899 http://dx.doi.org/10.1155/2018/3698078 Text en Copyright © 2018 Vincenzo Giancotti et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Giancotti, Vincenzo Bergamin, Natascha Cataldi, Palmina Rizzi, Claudio Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties |
title | Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties |
title_full | Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties |
title_fullStr | Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties |
title_full_unstemmed | Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties |
title_short | Epigenetic Contribution of High-Mobility Group A Proteins to Stem Cell Properties |
title_sort | epigenetic contribution of high-mobility group a proteins to stem cell properties |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941823/ https://www.ncbi.nlm.nih.gov/pubmed/29853899 http://dx.doi.org/10.1155/2018/3698078 |
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