Pamidimukkala Nidhi V, Leonard Mary Kathryn, Snyder Devin, McCorkle Joseph R, Kaetzel David M
Department of Biochemistry and Molecular Biology, School of Medicine, University of Maryland-Baltimore, Baltimore, MD, U.S.A.
Markey Cancer Center, University of Kentucky, Lexington, KY, U.S.A.
Anticancer Res. 2018 Nov;38(11):6059-6068. doi: 10.21873/anticanres.12956.
BACKGROUND/AIM: NME/NM23 nucleoside diphosphate kinase 1 (NME1) is a metastasis suppressor gene, exhibiting reduced expression in metastatic cancers and the ability to suppress metastatic activity of cancer cells. We previously identified NME1-regulated genes with prognostic value in human melanoma. This study was conducted in melanoma cell lines aiming to elucidate the mechanism through which NME regulates one of these genes, aldolase C (ALDOC).
ALDOC mRNA and protein expression was measured using qRT-PCR and immunoblot analyses. Promoter-luciferase constructs and chromatin immunoprecipitation were employed to measure the impact of NME1 on ALDOC transcription.
NME1 enhanced ALDOC transcription, evidenced by increased expression of ALDOC pre-mRNA and activity of an ALDOC promoter-luciferase module. NME1 was detected at the ALDOC promoter, and forced NME1 expression resulted in enhanced occupancy of the promoter by NME1, increased presence of epigenetic activation markers (H3K4me3 and H3K27ac), and recruitment of RNA polymerase II.
This is the first study to indicate that NME1 induces transcription through its direct binding to the promoter region of a target gene.
背景/目的:NME/NM23核苷二磷酸激酶1(NME1)是一种转移抑制基因,在转移性癌症中表达降低,并具有抑制癌细胞转移活性的能力。我们之前在人类黑色素瘤中鉴定出具有预后价值的NME1调控基因。本研究在黑色素瘤细胞系中进行,旨在阐明NME调控其中一个基因醛缩酶C(ALDOC)的机制。
使用qRT-PCR和免疫印迹分析测量ALDOC mRNA和蛋白表达。采用启动子-荧光素酶构建体和染色质免疫沉淀来测量NME1对ALDOC转录的影响。
NME1增强了ALDOC转录,这通过ALDOC前体mRNA表达增加和ALDOC启动子-荧光素酶模块活性增加得到证明。在ALDOC启动子处检测到NME1,强制表达NME1导致NME1对启动子的占据增加、表观遗传激活标记(H3K4me3和H3K27ac)的存在增加以及RNA聚合酶II的募集。
这是第一项表明NME1通过直接结合靶基因启动子区域诱导转录的研究。