Ray Mukulika, Singh Gunjan, Lakhotia Subhash C
Cytogenetics Laboratory, Department of Zoology, Banaras Hindu University, Varanasi, 221005, India.
Gene Expr Patterns. 2019 Sep;33:20-36. doi: 10.1016/j.gep.2019.05.002. Epub 2019 May 13.
We exploited the high Ras activity induced differentiation of supernumerary R7 cells in Drosophila eyes to examine if hsrω lncRNAs influence active Ras signaling. Surprisingly, either down- or up-regulation of hsrω lncRNAs in sev-GAL4>Ras expressing eye discs resulted in complete pupal lethality and substantially greater increase in R7 photoreceptor number at the expense of cone cells. Enhanced nuclear p-MAPK and presence of sev-GAL4 driven Ras bound RafRBDFLAG in cells not expressing the sev-GAL4 driver indicated non-cell autonomous spread of Ras signaling when hsrω levels were co-altered. RNA-sequencing revealed that down-and up-regulation of hsrω transcripts in sev-GAL4>Ras expressing eye discs elevated transcripts of positive or negative modulators, respectively, of Ras signaling so that either condition enhances it. Altered hsrω transcript levels in sev-GAL4>Ras expressing discs also affected sn/sno/sca RNAs and some other RNA processing transcript levels. Post-transcriptional changes due to the disrupted intra-cellular dynamicity of omega speckle associated hnRNPs and other RNA-binding proteins that follow down- or up-regulation of hsrω lncRNAs appear to be responsible for the further elevated Ras signaling. Cell autonomous and non-autonomous enhancement of Ras signaling by lncRNAs like hsrω has implications for cell signaling during high Ras activity commonly associated with some cancers.
我们利用果蝇眼中过量R7细胞因Ras活性高而诱导分化的现象,来研究hsrω长链非编码RNA(lncRNAs)是否影响活跃的Ras信号传导。令人惊讶的是,在sev-GAL4>Ras表达的眼盘中,hsrω lncRNAs的下调或上调均导致完全的蛹期致死率,并以锥体细胞为代价,使R7光感受器数量大幅增加。在不表达sev-GAL4驱动子的细胞中,增强的核磷酸化丝裂原活化蛋白激酶(p-MAPK)以及sev-GAL4驱动的Ras与RafRBDFLAG的结合表明,当hsrω水平共同改变时,Ras信号传导存在非细胞自主性扩散。RNA测序显示,在sev-GAL4>Ras表达的眼盘中,hsrω转录本的下调和上调分别提高了Ras信号传导的正向或负向调节因子的转录本水平,因此两种情况都会增强Ras信号传导。在sev-GAL4>Ras表达的盘中,hsrω转录本水平的改变也影响了sn/sno/sca RNA和其他一些RNA加工转录本水平。由于hsrω lncRNAs下调或上调后,与ω斑点相关的不均一核糖核蛋白(hnRNPs)和其他RNA结合蛋白的细胞内动态性被破坏而导致的转录后变化,似乎是Ras信号进一步增强的原因。像hsrω这样的lncRNAs对Ras信号传导的细胞自主性和非自主性增强,对于通常与某些癌症相关的高Ras活性期间的细胞信号传导具有重要意义。