Bunch Heeyoun, Lawney Brian P, Burkholder Adam, Ma Duanduan, Zheng Xiaofeng, Motola Shmulik, Fargo David C, Levine Stuart S, Wang Yaoyu E, Hu Guang
Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Center for Cancer Computational Biology, Dana Farber Cancer Institute, Boston, MA 02130, USA.
Genomics. 2016 Aug;108(2):64-77. doi: 10.1016/j.ygeno.2016.07.003. Epub 2016 Jul 16.
Mammalian genomes encode a large number of non-coding RNAs (ncRNAs) that greatly exceed mRNA genes. While the physiological and pathological roles of ncRNAs have been increasingly understood, the mechanisms of regulation of ncRNA expression are less clear. Here, our genomic study has shown that a significant number of long non-coding RNAs (lncRNAs, >1000 nucleotides) harbor RNA polymerase II (Pol II) engaged with the transcriptional start site. A pausing and transcriptional elongation factor for protein-coding genes, tripartite motif-containing 28 (TRIM28) regulates the transcription of a subset of lncRNAs in mammalian cells. In addition, the majority of lncRNAs in human and murine cells regulated by Pol II promoter-proximal pausing appear to function in stimulus-inducible biological pathways. Our findings suggest an important role of Pol II pausing for the transcription of mammalian lncRNA genes.
哺乳动物基因组编码大量非编码RNA(ncRNA),其数量大大超过mRNA基因。虽然人们对ncRNA的生理和病理作用的了解越来越多,但ncRNA表达的调控机制尚不清楚。在这里,我们的基因组研究表明,大量长链非编码RNA(lncRNA,>1000个核苷酸)含有与转录起始位点结合的RNA聚合酶II(Pol II)。一种用于蛋白质编码基因的暂停和转录延伸因子,含三联体基序的28(TRIM28),可调节哺乳动物细胞中一部分lncRNA的转录。此外,在人和小鼠细胞中,受Pol II启动子近端暂停调控的大多数lncRNA似乎在刺激诱导的生物学途径中发挥作用。我们的研究结果表明,Pol II暂停在哺乳动物lncRNA基因转录中具有重要作用。