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TET Methylcytosine Oxidases in T Cell and B Cell Development and Function

DNA methylation is established by DNA methyltransferases and is a key epigenetic mark. Ten-eleven translocation (TET) proteins are enzymes that oxidize 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and further oxidization products (oxi-mCs), which indirectly promote DNA demethylation. Her...

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Autores principales: Tsagaratou, Ageliki, Lio, Chan-Wang J., Yue, Xiaojing, Rao, Anjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374156/
https://www.ncbi.nlm.nih.gov/pubmed/28408905
http://dx.doi.org/10.3389/fimmu.2017.00220
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author Tsagaratou, Ageliki
Lio, Chan-Wang J.
Yue, Xiaojing
Rao, Anjana
author_facet Tsagaratou, Ageliki
Lio, Chan-Wang J.
Yue, Xiaojing
Rao, Anjana
author_sort Tsagaratou, Ageliki
collection PubMed
description DNA methylation is established by DNA methyltransferases and is a key epigenetic mark. Ten-eleven translocation (TET) proteins are enzymes that oxidize 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and further oxidization products (oxi-mCs), which indirectly promote DNA demethylation. Here, we provide an overview of the effect of TET proteins and altered DNA modification status in T and B cell development and function. We summarize current advances in our understanding of the role of TET proteins and 5hmC in T and B cells in both physiological and pathological contexts. We describe how TET proteins and 5hmC regulate DNA modification, chromatin accessibility, gene expression, and transcriptional networks and discuss potential underlying mechanisms and open questions in the field.
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spelling pubmed-53741562017-04-13 TET Methylcytosine Oxidases in T Cell and B Cell Development and Function Tsagaratou, Ageliki Lio, Chan-Wang J. Yue, Xiaojing Rao, Anjana Front Immunol Immunology DNA methylation is established by DNA methyltransferases and is a key epigenetic mark. Ten-eleven translocation (TET) proteins are enzymes that oxidize 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and further oxidization products (oxi-mCs), which indirectly promote DNA demethylation. Here, we provide an overview of the effect of TET proteins and altered DNA modification status in T and B cell development and function. We summarize current advances in our understanding of the role of TET proteins and 5hmC in T and B cells in both physiological and pathological contexts. We describe how TET proteins and 5hmC regulate DNA modification, chromatin accessibility, gene expression, and transcriptional networks and discuss potential underlying mechanisms and open questions in the field. Frontiers Media S.A. 2017-03-31 /pmc/articles/PMC5374156/ /pubmed/28408905 http://dx.doi.org/10.3389/fimmu.2017.00220 Text en Copyright © 2017 Tsagaratou, Lio, Yue and Rao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Tsagaratou, Ageliki
Lio, Chan-Wang J.
Yue, Xiaojing
Rao, Anjana
TET Methylcytosine Oxidases in T Cell and B Cell Development and Function
title TET Methylcytosine Oxidases in T Cell and B Cell Development and Function
title_full TET Methylcytosine Oxidases in T Cell and B Cell Development and Function
title_fullStr TET Methylcytosine Oxidases in T Cell and B Cell Development and Function
title_full_unstemmed TET Methylcytosine Oxidases in T Cell and B Cell Development and Function
title_short TET Methylcytosine Oxidases in T Cell and B Cell Development and Function
title_sort tet methylcytosine oxidases in t cell and b cell development and function
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374156/
https://www.ncbi.nlm.nih.gov/pubmed/28408905
http://dx.doi.org/10.3389/fimmu.2017.00220
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