Nagasaka Mai, Tsuzuki Kaori, Ozeki Yu, Tokugawa Muneshige, Ohoka Nobumichi, Inoue Yasumichi, Hayashi Hidetoshi
Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University.
Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences.
Biol Pharm Bull. 2019;42(3):481-488. doi: 10.1248/bpb.b18-00892.
Lysine-specific demethylase 1 (LSD1/KDM1A) is a histone demethylase and specifically catalyzes the demethylation of mono- and di-methylated histone H3 lysine 4 (H3K4). The LSD1-mediated demethylation of H3K4 promotes the assembly of the c-Myc-induced transcription initiation complex. Although LSD1 and c-Myc are both strongly expressed in human cancers, the mechanisms by which their activities are coordinated remain unclear. We herein demonstrated that LSD1 is a direct target gene of c-Myc. The knockdown of c-Myc decreased the expression of LSD1 in several cancer cell lines. We identified two non-canonical E-boxes in the proximal promoter region of the LSD1 gene. A chromatin immunoprecipitation assay showed that c-Myc bound to these E-boxes in the LSD1 promoter. Importantly, LSD1 mRNA expression correlated with c-Myc expression in human acute myeloid leukemia (AML), glioblastoma, stomach adenocarcinoma, and prostate adenocarcinoma. The present results suggest that LSD1 is induced by c-Myc and forms a positive feedback mechanism in transcription reactions by c-Myc.
赖氨酸特异性去甲基化酶1(LSD1/KDM1A)是一种组蛋白去甲基化酶,特异性催化单甲基化和二甲基化组蛋白H3赖氨酸4(H3K4)的去甲基化。LSD1介导的H3K4去甲基化促进c-Myc诱导的转录起始复合物的组装。尽管LSD1和c-Myc在人类癌症中均高表达,但其活性协同调控的机制仍不清楚。我们在此证明LSD1是c-Myc的直接靶基因。在多种癌细胞系中,敲低c-Myc可降低LSD1的表达。我们在LSD1基因的近端启动子区域鉴定出两个非典型E盒。染色质免疫沉淀试验表明,c-Myc与LSD1启动子中的这些E盒结合。重要的是,在人类急性髓系白血病(AML)、胶质母细胞瘤、胃腺癌和前列腺腺癌中,LSD1 mRNA表达与c-Myc表达相关。目前的结果表明,LSD1由c-Myc诱导,并在c-Myc的转录反应中形成正反馈机制。