Yale Stem Cell Center and Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06520.
Proc Natl Acad Sci U S A. 2014 Jan 7;111(1):337-42. doi: 10.1073/pnas.1320965111. Epub 2013 Dec 23.
PIWI proteins and their bound PIWI-interacting RNAs (piRNAs) are found in animal germlines and are essential for fertility, but their functions outside of the gonad are not well understood. The cnidarian Hydra is a simple metazoan with well-characterized stem/progenitor cells that provides a unique model for analysis of PIWI function. Here we report that Hydra has two PIWI proteins, Hydra PIWI (Hywi) and Hydra PIWI-like (Hyli), both of which are expressed in all Hydra stem/progenitor cells, but not in terminally differentiated cells. We identified ∼15 million piRNAs associated with Hywi and/or Hyli and found that they exhibit the ping-pong signature of piRNA biogenesis. Hydra PIWI proteins are strictly cytoplasmic and thus likely act as posttranscriptional regulators. To explore this function, we generated a Hydra transcriptome for piRNA mapping. piRNAs map to transposons with a 25- to 35-fold enrichment compared with the abundance of transposon transcripts. By sequencing the small RNAs specific to the interstitial, ectodermal, and endodermal lineages, we found that the targeting of transposons appears to be largely restricted to the interstitial lineage. We also identified putative nontransposon targets of the pathway unique to each lineage. Finally we demonstrate that hywi function is essential in the somatic epithelial lineages. This comprehensive analysis of the PIWI-piRNA pathway in the somatic stem/progenitor cells of a nonbilaterian animal suggests that this pathway originated with broader stem cell functionality.
PIWI 蛋白及其结合的 PIWI 相互作用 RNA(piRNA)存在于动物生殖细胞中,对生育能力至关重要,但它们在性腺外的功能尚不清楚。刺胞动物水螅是一种具有特征明确的干细胞/祖细胞的简单后生动物,为分析 PIWI 功能提供了独特的模型。在这里,我们报告水螅有两种 PIWI 蛋白,水螅 PIWI(Hywi)和水螅 PIWI 样(Hyli),它们都在所有水螅干细胞/祖细胞中表达,但不在终末分化细胞中表达。我们鉴定了约 1500 万个与 Hywi 和/或 Hyli 相关的 piRNA,并发现它们表现出 piRNA 生物发生的乒乓特征。水螅 PIWI 蛋白严格存在于细胞质中,因此可能作为转录后调节剂发挥作用。为了探索这种功能,我们生成了水螅 piRNA 映射转录组。与转座子转录本的丰度相比,piRNA 映射到转座子的丰度增加了 25-35 倍。通过对间质、外胚层和内胚层谱系特异性小 RNA 的测序,我们发现转座子的靶向似乎主要局限于间质谱系。我们还鉴定了每个谱系特有的通路的潜在非转座子靶标。最后,我们证明 hywi 功能在体腔上皮谱系中是必需的。对非双侧动物体腔干细胞/祖细胞中 PIWI-piRNA 通路的全面分析表明,该通路起源于更广泛的干细胞功能。