Life Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Department of Biology, Johns Hopkins University, Baltimore, Maryland, United States of America.
PLoS Genet. 2020 Mar 13;16(3):e1008648. doi: 10.1371/journal.pgen.1008648. eCollection 2020 Mar.
The piRNA pathway protects germline genomes from selfish genetic elements (e.g. transposons) through their transcript cleavage in the cytoplasm and/or their transcriptional silencing in the nucleus. Here, we describe a mechanism by which the nuclear and cytoplasmic arms of the piRNA pathway are linked. We find that during mitosis of Drosophila spermatogonia, nuclear Piwi interacts with nuage, the compartment that mediates the cytoplasmic arm of the piRNA pathway. At the end of mitosis, Piwi leaves nuage to return to the nucleus. Dissociation of Piwi from nuage occurs at the depolymerizing microtubules of the central spindle, mediated by a microtubule-depolymerizing kinesin, Klp10A. Depletion of klp10A delays the return of Piwi to the nucleus and affects piRNA production, suggesting the role of nuclear-cytoplasmic communication in piRNA biogenesis. We propose that cell cycle-dependent communication between the nuclear and cytoplasmic arms of the piRNA pathway may play a previously unappreciated role in piRNA regulation.
piRNA 通路通过在细胞质中切割其转录本和/或在核中沉默转录来保护生殖系基因组免受自私遗传元件(例如转座子)的侵害。在这里,我们描述了 piRNA 通路的核和细胞质臂相连的机制。我们发现,在果蝇精原细胞有丝分裂期间,核 Piwi 与介导 piRNA 通路细胞质臂的核质区室 nuage 相互作用。有丝分裂末期,Piwi 离开 nuage 回到核内。Piwi 从 nuage 上的解离发生在中心纺锤体的解聚微管上,由微管解聚驱动蛋白 Klp10A 介导。klp10A 的耗竭会延迟 Piwi 回到核内并影响 piRNA 的产生,表明核质通讯在 piRNA 生物发生中的作用。我们提出,piRNA 通路的核和细胞质臂之间的细胞周期依赖性通讯可能在 piRNA 调控中发挥了以前未被认识到的作用。