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A Novel Function of TET2 in CNS: Sustaining Neuronal Survival

DNA dioxygenases Ten-Eleven Translocation (TET) proteins can catalyze the conversion of 5-methylcytosine (5mC) of DNA to 5-hydroxymethylcytosine (5hmC), and thereby alter the epigenetic state of DNA. The TET family includes TET1, TET2 and TET3 members in mammals. Recently, accumulative research unco...

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Autores principales: Mi, Yajing, Gao, Xingchun, Dai, Jinxiang, Ma, Yue, Xu, Lixian, Jin, Weilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613284/
https://www.ncbi.nlm.nih.gov/pubmed/26378518
http://dx.doi.org/10.3390/ijms160921846
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author Mi, Yajing
Gao, Xingchun
Dai, Jinxiang
Ma, Yue
Xu, Lixian
Jin, Weilin
author_facet Mi, Yajing
Gao, Xingchun
Dai, Jinxiang
Ma, Yue
Xu, Lixian
Jin, Weilin
author_sort Mi, Yajing
collection PubMed
description DNA dioxygenases Ten-Eleven Translocation (TET) proteins can catalyze the conversion of 5-methylcytosine (5mC) of DNA to 5-hydroxymethylcytosine (5hmC), and thereby alter the epigenetic state of DNA. The TET family includes TET1, TET2 and TET3 members in mammals. Recently, accumulative research uncovered that TET1–3 occur abundantly in the central nervous system (CNS), and their biological functions have just begun to be investigated. In the present study, we demonstrated that mRNA and protein of TET2 were highly expressed in the cerebral cortex and hippocampus along the whole brain-development process. Further studies showed that TET2 was expressed in various types of cells, especially in most neurons. Subcellular distribution pattern implicated that TET2 is localized in both nucleus and cytoplasm of neurons. Down-regulation of TET2 in cultured cortical neurons with RNA interference implied that TET2 was required for cell survival. In all, our results indicate that neuronal TET2 is positively involved in the regulation of cell survival.
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spelling pubmed-46132842015-10-26 A Novel Function of TET2 in CNS: Sustaining Neuronal Survival Mi, Yajing Gao, Xingchun Dai, Jinxiang Ma, Yue Xu, Lixian Jin, Weilin Int J Mol Sci Article DNA dioxygenases Ten-Eleven Translocation (TET) proteins can catalyze the conversion of 5-methylcytosine (5mC) of DNA to 5-hydroxymethylcytosine (5hmC), and thereby alter the epigenetic state of DNA. The TET family includes TET1, TET2 and TET3 members in mammals. Recently, accumulative research uncovered that TET1–3 occur abundantly in the central nervous system (CNS), and their biological functions have just begun to be investigated. In the present study, we demonstrated that mRNA and protein of TET2 were highly expressed in the cerebral cortex and hippocampus along the whole brain-development process. Further studies showed that TET2 was expressed in various types of cells, especially in most neurons. Subcellular distribution pattern implicated that TET2 is localized in both nucleus and cytoplasm of neurons. Down-regulation of TET2 in cultured cortical neurons with RNA interference implied that TET2 was required for cell survival. In all, our results indicate that neuronal TET2 is positively involved in the regulation of cell survival. MDPI 2015-09-10 /pmc/articles/PMC4613284/ /pubmed/26378518 http://dx.doi.org/10.3390/ijms160921846 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mi, Yajing
Gao, Xingchun
Dai, Jinxiang
Ma, Yue
Xu, Lixian
Jin, Weilin
A Novel Function of TET2 in CNS: Sustaining Neuronal Survival
title A Novel Function of TET2 in CNS: Sustaining Neuronal Survival
title_full A Novel Function of TET2 in CNS: Sustaining Neuronal Survival
title_fullStr A Novel Function of TET2 in CNS: Sustaining Neuronal Survival
title_full_unstemmed A Novel Function of TET2 in CNS: Sustaining Neuronal Survival
title_short A Novel Function of TET2 in CNS: Sustaining Neuronal Survival
title_sort novel function of tet2 in cns: sustaining neuronal survival
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613284/
https://www.ncbi.nlm.nih.gov/pubmed/26378518
http://dx.doi.org/10.3390/ijms160921846
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