生物
RNA聚合酶Ⅱ
小核RNA
核糖核酸
RNA聚合酶Ⅱ全酶
一般转录因子
抄写(语言学)
RNA聚合酶Ⅲ
RNA聚合酶Ⅰ
聚四氟乙烯
分子生物学
转录因子ⅡD
细胞生物学
转录因子ⅡB
非编码RNA
RNA依赖性RNA聚合酶
基因表达
生物化学
发起人
基因
语言学
哲学
作者
Yuzhi Wang,Conner M. Traugot,Jodi L. Bubenik,Tianqi Li,Peike Sheng,Nicholas M. Hiers,Paul Fernández,Lu Li,Jiang Bian,Maurice S. Swanson,Mingyi Xie
出处
期刊:Molecular Cell
[Elsevier]
日期:2023-11-01
卷期号:83 (21): 3818-3834.e7
被引量:5
标识
DOI:10.1016/j.molcel.2023.09.020
摘要
N6-methyladenosine (m6A) modifications play crucial roles in RNA metabolism. How m6A regulates RNA polymerase II (RNA Pol II) transcription remains unclear. We find that 7SK small nuclear RNA (snRNA), a regulator of RNA Pol II promoter-proximal pausing, is highly m6A-modified in non-small cell lung cancer (NSCLC) cells. In A549 cells, we identified eight m6A sites on 7SK and discovered methyltransferase-like 3 (METTL3) and alkB homolog 5 (ALKBH5) as the responsible writer and eraser. When the m6A-7SK is specifically erased by a dCasRx-ALKBH5 fusion protein, A549 cell growth is attenuated due to reduction of RNA Pol II transcription. Mechanistically, removal of m6A leads to 7SK structural rearrangements that facilitate sequestration of the positive transcription elongation factor b (P-TEFb) complex, which results in reduction of serine 2 phosphorylation (Ser2P) in the RNA Pol II C-terminal domain and accumulation of RNA Pol II in the promoter-proximal region. Taken together, we uncover that m6A modifications of a non-coding RNA regulate RNA Pol II transcription and NSCLC tumorigenesis.
科研通智能强力驱动
Strongly Powered by AbleSci AI