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首页> 外文期刊>Nature neuroscience >The DNA modification N6-methyl-2 '-eoxyadenosine (m6dA) drives activity-induced gene expression and is required for fear extinction
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The DNA modification N6-methyl-2 '-eoxyadenosine (m6dA) drives activity-induced gene expression and is required for fear extinction

机译:DNA改性N6-甲基-2'-氧基腺苷(M6DA)驱动活性诱导的基因表达,是恐惧灭绝所需的

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摘要

DNA modification is known to regulate experience-dependent gene expression. However, beyond cytosine methylation and its oxidated derivatives, very little is known about the functional importance of chemical modifications on other nucleobases in the brain. Here we report that in adult mice trained in fear extinction, the DNA modification N6-methyl-2'-deoxyadenosine (m6dA) accumulates along promoters and coding sequences in activated prefrontal cortical neurons. The deposition of m6dA is associated with increased genome-wide occupancy of the mammalian m6dA methyltransferase, N6amt1, and this correlates with extinction-induced gene expression. The accumulation of m6dA is associated with transcriptional activation at the brain-derived neurotrophic factor (Bdnf) P4 promoter, which is required for Bdnf exon IV messenger RNA expression and for the extinction of conditioned fear. These results expand the scope of DNA modifications in the adult brain and highlight changes in m6dA as an epigenetic mechanism associated with activity-induced gene expression and the formation of fear extinction memory.
机译:已知DNA改性调节经验依赖性基因表达。然而,除了胞嘧啶甲基化及其氧化衍生物之外,关于脑中其他核碱基对其他核碱基的功能性重要性毫无少。在这里,我们认为,在恐惧灭绝的成年小鼠中,DNA改性N6-甲基-2'-脱氧腺苷(M6DA)沿激活前额相皮质神经元的启动子积累和编码序列。 M6DA的沉积与哺乳动物M6DA甲基转移酶,N6AMT1的基因组宽占状含量增加相关,并且这种与消失诱导的基因表达相关。 M6DA的累积与脑衍生的神经营养因子(BDNF)P4启动子的转录激活相关,这对于BDNF外显子IV信使RNA表达需要并灭绝条件恐惧。这些结果扩展了成年脑中的DNA修饰的范围,并突出M6DA的变化作为与活动诱导的基因表达相关的表观遗传机制以及恐惧消光记忆的形成。

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  • 来源
    《Nature neuroscience 》 |2019年第4期| 共14页
  • 作者单位

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Calif Los Angeles David Geffen Sch Med Intellectual Dev &

    Disabil Res Ctr Los Angeles CA;

    Univ Calif Irvine Dept Comp Sci Irvine CA USA;

    Univ Calif Irvine Dept Neurobiol &

    Behav Irvine CA USA;

    Pontificia Univ Catolica Rio Grande do Sul Brain Inst Porto Alegre RS Brazil;

    Pontificia Univ Catolica Rio Grande do Sul Brain Inst Porto Alegre RS Brazil;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Calif Irvine Dept Pharmaceut Sci Irvine CA USA;

    Norwegian Univ Sci &

    Technol Dept Canc Res &

    Mol Med Trondheim Norway;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

    Univ Calif Irvine Dept Pharmaceut Sci Irvine CA USA;

    Pontificia Univ Catolica Rio Grande do Sul Brain Inst Porto Alegre RS Brazil;

    Norwegian Univ Sci &

    Technol Dept Canc Res &

    Mol Med Trondheim Norway;

    Univ Calif Irvine Dept Comp Sci Irvine CA USA;

    Univ Calif Irvine Dept Pharmaceut Sci Irvine CA USA;

    Univ Queensland Queensland Brain Inst Cognit Neuroepigenet Lab Brisbane Qld Australia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 人体生理学 ;
  • 关键词

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