Hu Guangzhen, Lou Zhenkun, Gupta Mamta
Division of Hematology and Division of Oncology Research, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
PLoS One. 2014 Sep 8;9(9):e107016. doi: 10.1371/journal.pone.0107016. eCollection 2014.
Long noncoding RNAs (lncRNAs) are important regulators of transcription; however, their involvement in protein translation is not well known. Here we explored whether the lncRNA GAS5 is associated with translation initiation machinery and regulates translation. GAS5 was enriched with eukaryotic translation initiation factor-4E (eIF4E) in an RNA-immunoprecipitation assay using lymphoma cell lines. We identified two RNA binding motifs within eIF4E protein and the deletion of each motif inhibited the binding of GAS5 with eIF4E. To confirm the role of GAS5 in translation regulation, GAS5 siRNA and in vitro transcribed GAS5 RNA were used to knock down or overexpress GAS5, respectively. GAS5 siRNA had no effect on global protein translation but did specifically increase c-Myc protein level without an effect on c-Myc mRNA. The mechanism of this increase in c-Myc protein was enhanced association of c-Myc mRNA with the polysome without any effect on protein stability. In contrast, overexpression of in vitro transcribed GAS5 RNA suppressed c-Myc protein without affecting c-Myc mRNA. Interestingly, GAS5 was found to be bound with c-Myc mRNA, suggesting that GAS5 regulates c-Myc translation through lncRNA-mRNA interaction. Our findings have uncovered a role of GAS5 lncRNA in translation regulation through its interactions with eIF4E and c-Myc mRNA.
长链非编码RNA(lncRNAs)是转录的重要调节因子;然而,它们在蛋白质翻译中的作用尚不清楚。在此,我们探究了lncRNA GAS5是否与翻译起始机制相关并调节翻译。在使用淋巴瘤细胞系的RNA免疫沉淀实验中,GAS5与真核翻译起始因子4E(eIF4E)富集。我们在eIF4E蛋白中鉴定出两个RNA结合基序,每个基序的缺失均抑制了GAS5与eIF4E的结合。为了证实GAS5在翻译调控中的作用,分别使用GAS5 siRNA和体外转录的GAS5 RNA来敲低或过表达GAS5。GAS5 siRNA对整体蛋白质翻译无影响,但确实特异性增加了c-Myc蛋白水平,而对c-Myc mRNA无影响。c-Myc蛋白增加的机制是c-Myc mRNA与多核糖体的结合增强,而对蛋白质稳定性无任何影响。相反,体外转录的GAS5 RNA过表达抑制了c-Myc蛋白,而不影响c-Myc mRNA。有趣的是,发现GAS5与c-Myc mRNA结合,表明GAS5通过lncRNA-mRNA相互作用调节c-Myc翻译。我们的研究结果揭示了GAS5 lncRNA通过与eIF4E和c-Myc mRNA相互作用在翻译调控中的作用。