Alteration of genic 5-hydroxymethylcytosine patterning in olfactory neurons correlates with changes in gene expression and cell identity

被引:90
|
作者
Colquitt, Bradley M. [1 ]
Allen, William E. [2 ]
Barnea, Gilad [2 ]
Lomvardas, Stavros [3 ]
机构
[1] Univ Calif San Francisco, Grad Program Neurosci, San Francisco, CA 94158 USA
[2] Brown Univ, Dept Neurosci, Providence, RI 02912 USA
[3] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94158 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
epigenetics; olfaction; neurodevelopment; EMBRYONIC STEM-CELLS; DNA METHYLATION; NERVOUS-SYSTEM; MAMMALIAN DNA; TET PROTEINS; 5-METHYLCYTOSINE; MECP2; WIDE; 5-CARBOXYLCYTOSINE; DIFFERENTIATION;
D O I
10.1073/pnas.1302759110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The modified DNA base 5-hydroxymethylcytosine (5hmC) is enriched in neurons where it may contribute to gene regulation and cellular identity. To determine how 5hmC influences gene expression in an in vivo neuronal population, we assessed the patterning and function of the base along the developmental lineage of the main olfactory epithelium-from multipotent stem cells through neuronal progenitors to mature olfactory sensory neurons (mOSNs). We find that 5hmC increases over gene bodies during mOSN development with substantial patterning occuring between the progenitor and mOSN stages. Although gene-body 5hmC levels correlate with gene expression in all three developmental cell types, this association is particularly pronounced within mOSNs. Overexpression of Tet3 in mOSNs markedly alters gene-body 5hmC levels and gene expression in a manner consistent with a positive role for 5hmC in transcription. Moreover, Tet3 overexpression disrupts olfactory receptor expression and the targeting of axons to the olfactory bulb, key molecular and anatomical features of the olfactory system. Our results suggest a physiologically significant role for gene-body 5hmC in transcriptional facilitation and the maintenance of cellular identity independent of its function as an intermediate to demethylation.
引用
收藏
页码:14682 / 14687
页数:6
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