Department of Biochemistry, Purdue University, West Lafayette, Indiana, United States of America.
PLoS Biol. 2013 Nov;11(11):e1001715. doi: 10.1371/journal.pbio.1001715. Epub 2013 Nov 19.
Long noncoding RNAs (lncRNAs) are a class of molecules that impinge on the expression of protein-coding genes. Previous studies have suggested that the GAL cluster-associated lncRNAs of Saccharomyces cerevisiae repress expression of the protein-coding GAL genes. Herein, we demonstrate a previously unrecognized role for the GAL lncRNAs in activating gene expression. In yeast strains lacking the RNA helicase, DBP2, or the RNA decay enzyme, XRN1, we find that the GAL lncRNAs specifically accelerate gene expression from a prior repressive state. Furthermore, we provide evidence that the previously suggested repressive role is a result of specific mutant phenotypes, rather than a reflection of the normal, wild-type function of these noncoding RNAs. To shed light on the mechanism for lncRNA-dependent gene activation, we show that rapid induction of the protein-coding GAL genes is associated with faster recruitment of RNA polymerase II and reduced association of transcriptional repressors with GAL gene promoters. This suggests that the GAL lncRNAs enhance expression by derepressing the GAL genes. Consistently, the GAL lncRNAs enhance the kinetics of transcriptional induction, promoting faster expression of the protein-coding GAL genes upon the switch in carbon source. We suggest that the GAL lncRNAs poise inducible genes for rapid activation, enabling cells to more effectively trigger new transcriptional programs in response to cellular cues.
长非编码 RNA(lncRNA)是一类影响蛋白编码基因表达的分子。先前的研究表明,酿酒酵母 GAL 簇相关的 lncRNA 抑制蛋白编码 GAL 基因的表达。在此,我们证明了 GAL lncRNA 在激活基因表达方面具有以前未被认识到的作用。在缺乏 RNA 解旋酶 DBP2 或 RNA 降解酶 XRN1 的酵母菌株中,我们发现 GAL lncRNA 特异性地加速了先前抑制状态下基因的表达。此外,我们提供的证据表明,先前提出的抑制作用是特定突变表型的结果,而不是这些非编码 RNA 正常野生型功能的反映。为了阐明 lncRNA 依赖性基因激活的机制,我们表明,蛋白编码 GAL 基因的快速诱导与 RNA 聚合酶 II 的更快募集和转录抑制剂与 GAL 基因启动子的更少结合有关。这表明,GAL lncRNA 通过去抑制 GAL 基因来增强表达。一致地,GAL lncRNA 增强了转录诱导的动力学,在碳源切换时促进了蛋白编码 GAL 基因的更快表达。我们认为,GAL lncRNA 使可诱导基因处于快速激活的状态,使细胞能够更有效地响应细胞信号触发新的转录程序。