National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA; Oak Ridge Institute for Science and Education, US Department of Energy, Oak Ridge, TN, USA.
Cell Rep. 2024 Oct 22;43(10):114777. doi: 10.1016/j.celrep.2024.114777. Epub 2024 Sep 19.
PIWI-interacting RNAs (piRNAs) play a crucial role in safeguarding genome integrity by silencing mobile genetic elements. From flies to humans, piRNAs originate from long single-stranded precursors encoded by genomic piRNA clusters. How piRNA clusters form to adapt to genomic invaders and evolve to maintain protection remain key outstanding questions. Here, we generate a roadmap of piRNA clusters across seven species that highlights both similarities and variations. In mammals, we identify transcriptional readthrough as a mechanism to generate piRNAs from transposon insertions (piCs) downstream of genes (DoG). Together with the well-known stress-dependent DoG transcripts, our findings suggest a molecular mechanism for the formation of piRNA clusters in response to retroviral invasion. Finally, we identify a class of dynamic piRNA clusters in humans, underscoring unique features of human germ cell biology. Our results advance the understanding of conserved principles and species-specific variations in piRNA biology and provide tools for future studies.
PIWI 相互作用 RNA(piRNAs)通过沉默移动遗传元件在保护基因组完整性方面发挥着关键作用。从苍蝇到人类,piRNAs 来源于由基因组 piRNA 簇编码的长单链前体。piRNA 簇如何形成以适应基因组入侵并进化以维持保护仍然是关键的悬而未决的问题。在这里,我们生成了七个物种的 piRNA 簇图谱,突出了它们的相似性和差异。在哺乳动物中,我们发现转录通读是一种从基因下游的转座子插入(piCs)产生 piRNAs 的机制(DoG)。与众所周知的应激依赖型 DoG 转录本一起,我们的发现为针对逆转录病毒入侵形成 piRNA 簇的分子机制提供了线索。最后,我们在人类中鉴定出一类动态的 piRNA 簇,强调了人类生殖细胞生物学的独特特征。我们的研究结果推进了对 piRNA 生物学保守原则和物种特异性变异的理解,并为未来的研究提供了工具。