Institute of Molecular Biotechnology of the Austrian Academy of Sciences IMBA, 1030 Vienna, Austria.
Genes Dev. 2013 Aug 1;27(15):1693-705. doi: 10.1101/gad.221150.113.
The PIWI-interacting RNA (piRNA) pathway is a small RNA silencing system that keeps selfish genetic elements such as transposons under control in animal gonads. Several lines of evidence indicate that nuclear PIWI family proteins guide transcriptional silencing of their targets, yet the composition of the underlying silencing complex is unknown. Here we demonstrate that the double CHHC zinc finger protein gametocyte-specific factor 1 (Gtsf1) is an essential factor for Piwi-mediated transcriptional repression in Drosophila. Cells lacking Gtsf1 contain nuclear Piwi loaded with piRNAs, yet Piwi's silencing capacity is ablated. Gtsf1 interacts directly with a small subpool of nuclear Piwi, and loss of Gtsf1 phenocopies loss of Piwi in terms of deregulation of transposons, loss of H3K9 trimethylation (H3K9me3) marks at euchromatic transposon insertions, and deregulation of genes in proximity to repressed transposons. We propose that only a small fraction of nuclear Piwi is actively engaged in target silencing and that Gtsf1 is an essential component of the underlying Piwi-centered silencing complex.
PIWI 相互作用 RNA (piRNA) 途径是一种小 RNA 沉默系统,可控制动物生殖腺中的自私遗传元件,如转座子。有几条证据表明,核 PIWI 家族蛋白指导其靶标的转录沉默,但潜在沉默复合物的组成尚不清楚。在这里,我们证明双 CHHC 锌指蛋白配子细胞特异性因子 1 (Gtsf1) 是果蝇中 Piwi 介导的转录抑制所必需的因素。缺乏 Gtsf1 的细胞含有装载 piRNA 的核 Piwi,但 Piwi 的沉默能力被削弱。Gtsf1 与一小部分核 Piwi 直接相互作用,而 Gtsf1 的缺失在转座子失调、常染色质转座子插入处的 H3K9 三甲基化 (H3K9me3) 标记丢失以及靠近受抑制转座子的基因失调方面模拟了 Piwi 的缺失。我们提出,只有一小部分核 Piwi 积极参与靶标沉默,而 Gtsf1 是潜在的 Piwi 为中心的沉默复合物的重要组成部分。