Department of Cell Biology, Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
Department of Cell Biology, Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
Mol Cell. 2014 Jan 23;53(2):262-76. doi: 10.1016/j.molcel.2013.11.014. Epub 2013 Dec 26.
Endogenous small interfering RNAs (siRNAs) and other classes of small RNA provide the specificity signals for silencing of transposons and repeated DNA elements at the posttranscriptional and transcriptional levels. However, the determinants that define an siRNA-producing region or control the silencing function of siRNAs are poorly understood. Here we show that convergent antisense transcription and availability of the Dicer ribonuclease are the key determinants for primary siRNA generation. Surprisingly, Dicer makes dual contributions to heterochromatin formation, promoting histone H3 lysine 9 methylation independently of its catalytic activity, in addition to its well-known role in catalyzing siRNA generation. Furthermore, sequences in the 3' UTR of an mRNA-coding gene inhibit the ability of siRNAs to promote heterochromatin formation, providing another layer of control that prevents the silencing of protein-coding RNAs. Our results reveal distinct mechanisms that limit siRNA generation to centromeric DNA repeats and prevent spurious siRNA-mediated silencing at euchromatic loci.
内源性小干扰 RNA(siRNA)和其他种类的小 RNA 提供了转录后和转录水平上转座子和重复 DNA 元件沉默的特异性信号。然而,定义 siRNA 产生区域的决定因素或控制 siRNA 沉默功能的决定因素还知之甚少。在这里,我们表明,趋同反义转录和 Dicer 核糖核酸酶的可用性是产生初级 siRNA 的关键决定因素。令人惊讶的是,Dicer 除了其在催化 siRNA 生成中的作用外,还独立于其催化活性,对异染色质形成具有双重贡献,促进组蛋白 H3 赖氨酸 9 甲基化。此外,mRNA 编码基因 3'UTR 中的序列抑制 siRNA 促进异染色质形成的能力,提供了另一层防止蛋白编码 RNA 沉默的控制。我们的研究结果揭示了限制 siRNA 生成到着丝粒 DNA 重复序列并防止在常染色质位置发生虚假 siRNA 介导沉默的不同机制。