Department of Cell and Developmental Biology, Cancer center at Illinois, University of Illinois at Urbana-Champaign, Urbana, United States.
Department of BioHealth Informatics, School of Informatics and Computing, IUPUI, Indianapolis, United States.
Elife. 2020 Oct 27;9:e55102. doi: 10.7554/eLife.55102.
Cell cycle is a cellular process that is subject to stringent control. In contrast to the wealth of knowledge of proteins controlling the cell cycle, very little is known about the molecular role of lncRNAs (long noncoding RNAs) in cell-cycle progression. By performing genome-wide transcriptome analyses in cell-cycle-synchronized cells, we observed cell-cycle phase-specific induction of >2000 lncRNAs. Further, we demonstrate that an S-phase-upregulated lncRNA, , facilitates cell-cycle progression by promoting YAP1-mediated gene expression. facilitates the cell-cycle-specific transcription of , a positive regulator of YAP1, by promoting the co-activator, DDX5-mediated stabilization of RNA polymerase II on chromatin. Finally, elevated levels are associated with poor cancer prognosis and tumorigenicity, implying its pro-survival role. Thus, we demonstrate the role of a S-phase up-regulated lncRNA in cell-cycle progression modulating the expression of genes controlling cell proliferation.
细胞周期是一个受到严格控制的细胞过程。与控制细胞周期的蛋白质的丰富知识相比,lncRNAs(长非编码 RNA)在细胞周期进展中的分子作用知之甚少。通过在细胞周期同步化细胞中进行全基因组转录组分析,我们观察到 >2000 个 lncRNAs 具有细胞周期阶段特异性诱导。此外,我们证明了一个 S 期上调的 lncRNA ,通过促进 YAP1 介导的基因表达来促进细胞周期进程。 促进 YAP1 的正调节剂 的细胞周期特异性转录,通过促进共激活因子 DDX5 介导的 RNA 聚合酶 II 在染色质上的稳定。最后,升高的 水平与不良的癌症预后和致瘤性相关,暗示其具有生存促进作用。因此,我们证明了 S 期上调的 lncRNA 在细胞周期进展中调节控制细胞增殖的基因表达的作用。