生物
癌变
翻译(生物学)
信使核糖核酸
癌基因
细胞生物学
癌症研究
癌症
遗传学
基因
细胞周期
作者
Yunfeng Gao,Ming Jiang,Fangqin Guo,Xuejiao Liu,Qi Zhang,Sen Yang,Yiu To Yeung,Ran Yang,Keke Wang,Qiong Wu,Dandan Zhang,Chengjuan Zhang,Kyle Vaughn Laster,Ming Ge,Wenna Nie,Kangdong Liu,Zigang Dong
出处
期刊:Oncogene
[Springer Nature]
日期:2022-09-15
卷期号:41 (42): 4736-4753
被引量:7
标识
DOI:10.1038/s41388-022-02464-x
摘要
Abnormal translation of the MYC proto-oncogene is a hallmark of the initiation and maintenance of tumorigenesis. However, the molecular mechanism underlying increased MYC protein levels in certain cancer types without a corresponding increase in MYC mRNA levels is unclear. Here, we identified a novel lncRNA, MTAR1, which is critical for post-transcriptional regulation of MYC-induced tumorigenesis. MTAR1 is essential for recruiting IGF2BPs into PABP1-mediated liquid-liquid phase separation (LLPS) complexes and facilitates IGF2BPs-mediated MYC mRNA translation. MTAR1 enhanced binding between IGF2BPs and PABP1, thereby promoting MYC mRNA stability and increased MYC mRNA translation. In summary, MTAR1 is a novel MYC-related lncRNA that contributes to tumor progression by enhancing MYC translation through mediating PABP1/IGF2BPs liquid-liquid phase separation.
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