Shi Kun, Zhang Ying, Du Zhenzhen, Liu Symonne C, Fan Xinyu, Lee Heng-Chi, Zhang Donglei
Department of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430032, China.
These authors contribute equally.
bioRxiv. 2025 Jan 24:2025.01.23.634177. doi: 10.1101/2025.01.23.634177.
Animals have evolved distinct small RNA pathways, including piRNA and siRNA, to silence invasive and selfish nucleic acids. piRNA pathway factors are concentrated in perinuclear germ granules that frequently associate with nuclear pore complexes (NPCs). However, the factors mediating germ granule-NPC association and the functional relevance of such association remain unknown. Here we show that the conserved nucleoporins NPP-14 (NUP-214) and NPP-24 (NUP-88), components of the cytoplasmic filaments of NPC, play critical roles in anchoring germ granule to NPC and in attenuating piRNA silencing In . Proximity labeling experiments further identified EPS-1 (enhanced piRNA silencing) as a key germ granule factor contributing to germ granule-NPC interaction. In , or mutant animals, we observed fewer but enlarged, unorganized germ granules, accompanied by the over-amplification of secondary small RNAs at piRNA targeting sites. Nonetheless, we found this enhancement of piRNA silencing comes at the cost of dampened RNAi efficiency and RNAi inheritance. Together, our studies uncovered factors contributing to germ granule-NPC association and underscored the importance of spatial organization of germ granules in balancing small RNA silencing pathways.
动物已经进化出不同的小RNA途径,包括piRNA和siRNA,以沉默侵入性和自私的核酸。piRNA途径因子集中在经常与核孔复合体(NPC)相关联的核周生殖颗粒中。然而,介导生殖颗粒与NPC关联的因子以及这种关联的功能相关性仍然未知。在这里,我们表明保守的核孔蛋白NPP-14(NUP-214)和NPP-24(NUP-88),即NPC细胞质细丝的组成部分,在将生殖颗粒锚定到NPC以及减弱piRNA沉默中起关键作用。邻近标记实验进一步确定EPS-1(增强的piRNA沉默)是促进生殖颗粒与NPC相互作用的关键生殖颗粒因子。在npp-14、npp-24或eps-1突变动物中,我们观察到生殖颗粒数量减少但体积增大且无组织,同时在piRNA靶向位点处二级小RNA过度扩增。尽管如此,我们发现这种piRNA沉默的增强是以RNAi效率和RNAi遗传减弱为代价的。总之,我们的研究揭示了有助于生殖颗粒与NPC关联的因子,并强调了生殖颗粒的空间组织在平衡小RNA沉默途径中的重要性。