N6-methyladenosine in 7SK small nuclear RNA underlies RNA polymerase II transcription regulation

被引:7
|
作者
Wang, Yuzhi [1 ,2 ]
Traugot, Conner M. [1 ,2 ]
Bubenik, Jodi L. [3 ,4 ]
Li, Tianqi [1 ,2 ]
Sheng, Peike [1 ,2 ]
Hiers, Nicholas M. [1 ,2 ]
Fernandez, Paul [1 ,2 ]
Li, Lu [1 ,2 ]
Bian, Jiang [2 ,5 ]
Swanson, Maurice S. [3 ,4 ]
Xie, Mingyi [1 ,2 ,4 ]
机构
[1] Univ Florida, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
[2] Univ Florida, UF Hlth Canc Ctr, Gainesville, FL 32610 USA
[3] Univ Florida, Dept Mol Genet & Microbiol, Gainesville, FL 32610 USA
[4] Univ Florida, UF Genet Inst, Gainesville, FL 32610 USA
[5] Univ Florida, Dept Hlth Outcomes & Biomed Informat, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
MESSENGER-RNA; P-TEFB; M(6)A RNA; STRUCTURAL BASIS; NONCODING RNAS; METHYLATION; ELONGATION; SNRNP; HEXIM1; N-6-METHYLADENOSINE;
D O I
10.1016/j.molcel.2023.09.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
N6-methyladenosine (m6A) modifications play crucial roles in RNA metabolism. How m6A regulates RNA po-lymerase II (RNA Pol II) transcription remains unclear. We find that 7SK small nuclear RNA (snRNA), a regu-lator 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 transcrip-tion. 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 phos-phorylation (Ser2P) in the RNA Pol II C-terminal domain and accumulation of RNA Pol II in the promoter -prox-imal region. Taken together, we uncover that m6A modifications of a non-coding RNA regulate RNA Pol II transcription and NSCLC tumorigenesis.
引用
收藏
页码:3818 / +
页数:25
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