Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.
Elife. 2019 Jun 20;8:e47999. doi: 10.7554/eLife.47999.
The PIWI-interacting RNA (piRNA) pathway is a small RNA-based immune system that controls the expression of transposons and maintains genome integrity in animal gonads. In , piRNA-guided silencing is achieved, in part, via co-transcriptional repression of transposons by Piwi. This depends on Panoramix (Panx); however, precisely how an RNA binding event silences transcription remains to be determined. Here we show that Nuclear Export Factor 2 (Nxf2) and its co-factor, Nxt1, form a complex with Panx and are required for co-transcriptional silencing of transposons in somatic and germline cells of the ovary. Tethering of Nxf2 or Nxt1 to RNA results in silencing of target loci and the concomitant accumulation of repressive chromatin marks. Nxf2 and Panx proteins are mutually required for proper localization and stability. We mapped the protein domains crucial for the Nxf2/Panx complex formation and show that the amino-terminal portion of Panx is sufficient to induce transcriptional silencing.
PIWI 相互作用 RNA (piRNA) 通路是一种基于小 RNA 的免疫系统,可控制转座子的表达并维持动物性腺中的基因组完整性。在 中,piRNA 指导的沉默部分是通过 Piwi 对转座子进行共转录抑制来实现的。这取决于 Panoramix (Panx);然而,RNA 结合事件如何沉默转录仍有待确定。在这里,我们表明核输出因子 2 (Nxf2) 和其辅助因子 Nxt1 与 Panx 形成复合物,并且在卵巢的体细胞和生殖细胞中转录物的共转录沉默中是必需的。Nxf2 或 Nxt1 与 RNA 的连接导致靶位点的沉默和伴随的抑制性染色质标记的积累。Nxf2 和 Panx 蛋白相互需要以实现正确的定位和稳定性。我们绘制了对于 Nxf2/Panx 复合物形成至关重要的蛋白结构域,并表明 Panx 的氨基端部分足以诱导转录沉默。