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,Meng-Meng 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:13
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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