RNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Bioinformatics Program, Boston University, Boston, MA 02215, USA.
Cell. 2018 Feb 22;172(5):937-951.e18. doi: 10.1016/j.cell.2018.02.002. Epub 2018 Feb 15.
piRNAs (Piwi-interacting small RNAs) engage Piwi Argonautes to silence transposons and promote fertility in animal germlines. Genetic and computational studies have suggested that C. elegans piRNAs tolerate mismatched pairing and in principle could target every transcript. Here we employ in vivo cross-linking to identify transcriptome-wide interactions between piRNAs and target RNAs. We show that piRNAs engage all germline mRNAs and that piRNA binding follows microRNA-like pairing rules. Targeting correlates better with binding energy than with piRNA abundance, suggesting that piRNA concentration does not limit targeting. In mRNAs silenced by piRNAs, secondary small RNAs accumulate at the center and ends of piRNA binding sites. In germline-expressed mRNAs, however, targeting by the CSR-1 Argonaute correlates with reduced piRNA binding density and suppression of piRNA-associated secondary small RNAs. Our findings reveal physiologically important and nuanced regulation of individual piRNA targets and provide evidence for a comprehensive post-transcriptional regulatory step in germline gene expression.
piRNAs(Piwi 相互作用的小 RNA)与 Piwi Argonautes 结合沉默转座子,促进动物生殖细胞的生育能力。遗传和计算研究表明,秀丽隐杆线虫的 piRNAs 可以容忍错配配对,原则上可以靶向每一个转录本。在这里,我们采用体内交联的方法来鉴定 piRNAs 和靶 RNA 之间的全转录组相互作用。我们表明 piRNAs 与所有生殖系 mRNA 结合,并且 piRNA 结合遵循 miRNA 样配对规则。靶标与结合能的相关性优于 piRNA 丰度,这表明 piRNA 浓度不会限制靶标。在被 piRNAs 沉默的 mRNA 中,次级小 RNA 会在 piRNA 结合位点的中心和末端积累。然而,在生殖系表达的 mRNA 中,CSR-1 Argonaute 的靶向与 piRNA 结合密度降低以及抑制 piRNA 相关的次级小 RNA 有关。我们的研究结果揭示了单个 piRNA 靶标的生理上重要且细微的调控,并为生殖细胞基因表达中的全面转录后调控步骤提供了证据。