Department of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
Department of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA
Development. 2018 Oct 22;145(20):dev167346. doi: 10.1242/dev.167346.
Nuclear RNA interference provides a unique approach to the study of RNA-mediated transgenerational epigenetic inheritance. A paradox in the field is that expression of target loci is necessary for the initiation and maintenance of their silencing. How expression and repression are coordinated during animal development is poorly understood. To resolve this gap, we took imaging, deep-sequencing and genetic approaches towards delineating the developmental regulation and subcellular localization of RNA transcripts of two representative endogenous targets, the LTR retrotransposons Cer3 and Cer8. By examining wild-type worms and a collection of mutant strains, we found that the expression and silencing cycle of Cer3 and Cer8 is coupled with embryonic and germline development. Strikingly, endogenous targets exhibit a hallmark of nuclear enrichment of their RNA transcripts. In addition, germline and somatic repressions of Cer3 have different genetic requirements for three heterochromatin enzymes, MET-2, SET-25 and SET-32, in conjunction with the nuclear Argonaute protein HRDE-1. These results provide the first comprehensive cellular and developmental characterization of nuclear RNAi activities throughout the animal reproductive cycle.
核 RNA 干扰为研究 RNA 介导的跨代表观遗传遗传提供了一种独特的方法。该领域存在一个悖论,即靶基因座的表达对于其沉默的起始和维持是必要的。在动物发育过程中,如何协调表达和抑制尚不清楚。为了解决这一差距,我们采用成像、深度测序和遗传方法来描绘两个代表性内源性靶标(LTR 反转录转座子 Cer3 和 Cer8)的 RNA 转录本的发育调控和亚细胞定位。通过检查野生型蠕虫和一系列突变株,我们发现 Cer3 和 Cer8 的表达和沉默周期与胚胎和生殖系发育偶联。引人注目的是,内源性靶标表现出其 RNA 转录本在核内富集的特征。此外,Cer3 的生殖系和体细胞抑制需要三种异染色质酶(MET-2、SET-25 和 SET-32)以及核 Argonaute 蛋白 HRDE-1 的协同作用,具有不同的遗传要求。这些结果提供了核 RNAi 活性在整个动物生殖周期中的全面细胞和发育特征描述。