Yildirim Ozlem, Izgu Enver C, Damle Manashree, Chalei Vladislava, Ji Fei, Sadreyev Ruslan I, Szostak Jack W, Kingston Robert E
Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA; Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ 08854, USA.
Cell Rep. 2020 May 12;31(6):107629. doi: 10.1016/j.celrep.2020.107629.
Many proteins that are needed for progression through S-phase are produced from transcripts that peak in the S-phase, linking temporal expression of those proteins to the time that they are required in cell cycle. Here, we explore the potential roles of long non-coding RNAs in cell cycle progression. We use a sensitive click-chemistry approach to isolate nascent RNAs in a human cell line, and we identify more than 900 long non-coding RNAs (lncRNAs) whose synthesis peaks during the S-phase. More than 200 of these are long intergenic non-coding RNAs (lincRNAs) with S-phase-specific expression. We characterize three of these lincRNAs by knockdown and find that all three lincRNAs are required for appropriate S-phase progression. We infer that non-coding RNAs are key regulatory effectors during the cell cycle, acting on distinct regulatory networks, and herein, we provide a large catalog of candidate cell-cycle regulatory RNAs.
许多推动S期进程所需的蛋白质由在S期达到峰值的转录本产生,将这些蛋白质的时间表达与它们在细胞周期中所需的时间联系起来。在这里,我们探讨长链非编码RNA在细胞周期进程中的潜在作用。我们使用一种灵敏的点击化学方法在人类细胞系中分离新生RNA,并鉴定出900多种长链非编码RNA(lncRNA),其合成在S期达到峰值。其中200多种是具有S期特异性表达的长链基因间非编码RNA(lincRNA)。我们通过敲低来表征其中三种lincRNA,发现所有这三种lincRNA都是S期正常进程所必需的。我们推断非编码RNA是细胞周期中的关键调节效应物,作用于不同的调节网络,在此,我们提供了大量候选细胞周期调节RNA的目录。