The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan 5290002, Israel.
Institute of Nanotechnology, Bar-Ilan University, Ramat Gan 5290002, Israel.
Proc Natl Acad Sci U S A. 2017 Oct 17;114(42):E8837-E8846. doi: 10.1073/pnas.1707440114. Epub 2017 Oct 3.
Nuclear RNA interference (RNAi) is mediated by the canonical RNAi machinery and can lead to transcriptional silencing, transcriptional activation, or modulation of alternative splicing patterns. These effects transpire through changes in histone and DNA modifications via RNAi-mediated recruitment of chromatin-modifying enzymes. To prove that nuclear RNAi occurs and modulates transcription in human cells, we used live-cell imaging to detect and track nuclear RNAi transcriptional repression in single living human cells. While employing reporter genes constructed with inducible promoters and cognate-inducible short hairpin RNA (shRNA) targeted against the reporter coding region, we have characterized the dynamics of the nuclear RNAi process in living human cells. We show that the silencing effect is mediated through the nascent mRNA, followed by activity of histone methylating enzymes, but not through DNA methylation.
核 RNA 干扰 (RNAi) 是由经典的 RNAi 机制介导的,可导致转录沉默、转录激活或改变剪接模式。这些效应通过 RNAi 介导的染色质修饰酶募集导致组蛋白和 DNA 修饰的变化而发生。为了证明核 RNAi 在人类细胞中发生并调节转录,我们使用活细胞成像来检测和跟踪单个活人类细胞中的核 RNAi 转录抑制。在使用带有诱导启动子和针对报告基因编码区的同源诱导短发夹 RNA (shRNA) 的报告基因的同时,我们已经在活的人类细胞中表征了核 RNAi 过程的动力学。我们表明,沉默效应是通过新生 mRNA 介导的,随后是组蛋白甲基化酶的活性,但不是通过 DNA 甲基化。