Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells

<p>Abstract</p> <p>Background</p> <p>Pluripotent cells maintain a unique gene expression pattern and specific chromatin signature. In this study, we explored the effect of the methyltransferase inhibitor adenosine dialdehyde (AdOx) on pluripotency maintenance and gene e...

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Main Authors: Yan Li, Zhao Hai-yong, Zhang Ye, Shen Yu-fei
Format: Article
Language:English
Published: BMC 2012-01-01
Series:BMC Neuroscience
Online Access:http://www.biomedcentral.com/1471-2202/13/6
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spelling doaj-5bdea17f514a486590432a841ad2b2da2020-11-25T00:26:58ZengBMCBMC Neuroscience1471-22022012-01-01131610.1186/1471-2202-13-6Differential effects of AdOx on gene expression in P19 embryonal carcinoma cellsYan LiZhao Hai-yongZhang YeShen Yu-fei<p>Abstract</p> <p>Background</p> <p>Pluripotent cells maintain a unique gene expression pattern and specific chromatin signature. In this study, we explored the effect of the methyltransferase inhibitor adenosine dialdehyde (AdOx) on pluripotency maintenance and gene expression in P19 embryonal carcinoma cells.</p> <p>Results</p> <p>After AdOx treatment, the pluripotency-related gene network became disordered, and the early developmental genes were released from the repression. Remarkably, AdOx caused contrasting effects on the expression of two key pluripotency genes, <it>nanog </it>and <it>oct3/4</it>, with the reduction of the repressive histone marks H3K27me3, H3K9me3 and H3K9me2 only in the <it>nanog </it>gene.</p> <p>Conclusions</p> <p>Key pluripotency genes were controlled by different mechanisms, including the differential enrichment of repressive histone methylation marks. These data provided novel clues regarding the critical role of histone methylation in the maintenance of pluripotency and the determination of cell fate in P19 pluripotent cells.</p> http://www.biomedcentral.com/1471-2202/13/6
collection DOAJ
language English
format Article
sources DOAJ
author Yan Li
Zhao Hai-yong
Zhang Ye
Shen Yu-fei
spellingShingle Yan Li
Zhao Hai-yong
Zhang Ye
Shen Yu-fei
Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells
BMC Neuroscience
author_facet Yan Li
Zhao Hai-yong
Zhang Ye
Shen Yu-fei
author_sort Yan Li
title Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells
title_short Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells
title_full Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells
title_fullStr Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells
title_full_unstemmed Differential effects of AdOx on gene expression in P19 embryonal carcinoma cells
title_sort differential effects of adox on gene expression in p19 embryonal carcinoma cells
publisher BMC
series BMC Neuroscience
issn 1471-2202
publishDate 2012-01-01
description <p>Abstract</p> <p>Background</p> <p>Pluripotent cells maintain a unique gene expression pattern and specific chromatin signature. In this study, we explored the effect of the methyltransferase inhibitor adenosine dialdehyde (AdOx) on pluripotency maintenance and gene expression in P19 embryonal carcinoma cells.</p> <p>Results</p> <p>After AdOx treatment, the pluripotency-related gene network became disordered, and the early developmental genes were released from the repression. Remarkably, AdOx caused contrasting effects on the expression of two key pluripotency genes, <it>nanog </it>and <it>oct3/4</it>, with the reduction of the repressive histone marks H3K27me3, H3K9me3 and H3K9me2 only in the <it>nanog </it>gene.</p> <p>Conclusions</p> <p>Key pluripotency genes were controlled by different mechanisms, including the differential enrichment of repressive histone methylation marks. These data provided novel clues regarding the critical role of histone methylation in the maintenance of pluripotency and the determination of cell fate in P19 pluripotent cells.</p>
url http://www.biomedcentral.com/1471-2202/13/6
work_keys_str_mv AT yanli differentialeffectsofadoxongeneexpressioninp19embryonalcarcinomacells
AT zhaohaiyong differentialeffectsofadoxongeneexpressioninp19embryonalcarcinomacells
AT zhangye differentialeffectsofadoxongeneexpressioninp19embryonalcarcinomacells
AT shenyufei differentialeffectsofadoxongeneexpressioninp19embryonalcarcinomacells
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