Department of Neurobiology, Harvard Medical School, 220 Longwood Avenue, Boston, Massachusetts 02115, USA.
Nature. 2010 May 13;465(7295):182-7. doi: 10.1038/nature09033. Epub 2010 Apr 14.
We used genome-wide sequencing methods to study stimulus-dependent enhancer function in mouse cortical neurons. We identified approximately 12,000 neuronal activity-regulated enhancers that are bound by the general transcriptional co-activator CBP in an activity-dependent manner. A function of CBP at enhancers may be to recruit RNA polymerase II (RNAPII), as we also observed activity-regulated RNAPII binding to thousands of enhancers. Notably, RNAPII at enhancers transcribes bi-directionally a novel class of enhancer RNAs (eRNAs) within enhancer domains defined by the presence of histone H3 monomethylated at lysine 4. The level of eRNA expression at neuronal enhancers positively correlates with the level of messenger RNA synthesis at nearby genes, suggesting that eRNA synthesis occurs specifically at enhancers that are actively engaged in promoting mRNA synthesis. These findings reveal that a widespread mechanism of enhancer activation involves RNAPII binding and eRNA synthesis.
我们使用全基因组测序方法研究了小鼠皮质神经元中刺激依赖性增强子功能。我们鉴定出大约 12000 个神经元活性调节增强子,这些增强子通过 CBP 的活性依赖性方式结合一般转录共激活因子 CBP。CBP 在增强子上的一个功能可能是募集 RNA 聚合酶 II(RNAPII),因为我们还观察到活性调节的 RNAPII 结合到数千个增强子上。值得注意的是,RNAPII 在增强子上双向转录一个新的增强子 RNA(eRNA)类,这些增强子区域由存在组蛋白 H3 赖氨酸 4 单甲基化定义。神经元增强子上的 eRNA 表达水平与附近基因的信使 RNA 合成水平呈正相关,这表明 eRNA 合成发生在积极参与促进 mRNA 合成的增强子上。这些发现揭示了一种广泛的增强子激活机制,涉及 RNAPII 结合和 eRNA 合成。