生物
脱甲基酶
转录组
基因沉默
癌症研究
转录因子
细胞生物学
基因表达
甲基转移酶
干细胞
基因
福克斯M1
癌变
甲基化
表观遗传学
遗传学
作者
Sicong Zhang,Boxuan Simen Zhao,Aidong Zhou,Kangyu Lin,Suli Zheng,Zhike Lu,Yaohui Chen,Erik P. Sulman,Keping Xie,Oliver Bögler,Sadhan Majumder,Chuan He,Suyun Huang
出处
期刊:Cancer Cell
[Cell Press]
日期:2017-04-01
卷期号:31 (4): 591-606.e6
被引量:1182
标识
DOI:10.1016/j.ccell.2017.02.013
摘要
The dynamic and reversible N6-methyladenosine (m6A) RNA modification installed and erased by N6-methyltransferases and demethylases regulates gene expression and cell fate. We show that the m6A demethylase ALKBH5 is highly expressed in glioblastoma stem-like cells (GSCs). Silencing ALKBH5 suppresses the proliferation of patient-derived GSCs. Integrated transcriptome and m6A-seq analyses revealed altered expression of certain ALKBH5 target genes, including the transcription factor FOXM1. ALKBH5 demethylates FOXM1 nascent transcripts, leading to enhanced FOXM1 expression. Furthermore, a long non-coding RNA antisense to FOXM1 (FOXM1-AS) promotes the interaction of ALKBH5 with FOXM1 nascent transcripts. Depleting ALKBH5 and FOXM1-AS disrupted GSC tumorigenesis through the FOXM1 axis. Our work uncovers a critical function for ALKBH5 and provides insight into critical roles of m6A methylation in glioblastoma.
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