Department of Structural and Functional Biology, University of Naples 'Federico II', Naples, Italy.
Oncogene. 2010 Jun 24;29(25):3691-702. doi: 10.1038/onc.2010.120. Epub 2010 Apr 26.
Myc is a transcription factor that significantly contributes to cancer progression by modulating the expression of important genes through binding to a DNA sequence, CACGTG, called E-box. We find that on Myc binding to chromatin, the lysine-demethylating enzyme, LSD1, triggers a transient demethylation of lysine 4 in the histone H3. In addition, we demonstrate that Myc binds and recruits LSD1 to the E-box chromatin and the formation of this complex is stimulated by cAMP-PKA. Demethylation by LSD1 produces H(2)O(2), which locally oxidizes guanine and induces the recruitment of 8-oxoguanine-DNA glycosylase (OGG1) and of the nuclease Ape1 on the E-box chromatin. Inhibition of oxidation or silencing of LSD1, OGG1 or Ape1 significantly reduce transcription and inhibit mRNA accumulation of Myc-target genes. Collectively, these data highlight the role of transient LSD1-mediated demethylation of H3K4 leading to local DNA oxidation as driving force in the assembly of the Myc-induced transcription initiation complex.
Myc 是一种转录因子,通过与称为 E-box 的 DNA 序列 CACGTG 结合,调节重要基因的表达,从而显著促进癌症的进展。我们发现,在 Myc 与染色质结合时,赖氨酸去甲基化酶 LSD1 会引发组蛋白 H3 中赖氨酸 4 的瞬时去甲基化。此外,我们证明 Myc 结合并募集 LSD1 到 E-box 染色质,并且 cAMP-PKA 刺激这种复合物的形成。LSD1 的去甲基化产生 H2O2,它局部氧化鸟嘌呤并诱导 8-氧鸟嘌呤-DNA 糖基化酶 (OGG1) 和核酸内切酶 Ape1 在 E-box 染色质上的募集。氧化作用的抑制或 LSD1、OGG1 或 Ape1 的沉默显著降低 Myc 靶基因的转录和 mRNA 积累。总的来说,这些数据强调了 LSD1 介导的 H3K4 瞬时去甲基化导致局部 DNA 氧化作为 Myc 诱导的转录起始复合物组装的驱动力的作用。