Liu Simeiyun, Holmes Andrew D, Katzman Sol, Sharma Upasna
Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, California, 95064.
Genomics Institute, University of California, Santa Cruz, California, 95064.
bioRxiv. 2024 Aug 27:2024.08.08.607197. doi: 10.1101/2024.08.08.607197.
Sperm small RNAs have been implicated in intergenerational epigenetic inheritance of paternal environmental effects; however, their biogenesis and functions remain poorly understood. We previously identified a 5' fragment of tRNA-Valine-CAC-2 (tRFValCAC) as one of the most abundant small RNA in mature sperm. tRFValCAC is specifically enriched in sperm during post-testicular maturation in the epididymis, and we found that it is delivered to sperm from epididymis epithelial cells via extracellular vesicles. Here, we investigated the mechanistic basis of tRFValCAC delivery to sperm and its functions in the early embryo. We show that tRFValCAC interacts with an RNA binding protein, heterogeneous nuclear ribonucleoprotein A/B (hnRNPAB), in the epididymis, and this interaction regulates the sorting and packing of tRFValCAC into extracellular vesicles. In the embryo, we found that tRFValCAC regulates early embryonic mRNA processing and splicing. Inhibition of tRFValCAC in preimplantation embryos altered the transcript abundance of genes involved in RNA splicing and mRNA processing. Importantly, tRFValCAC-inhibited embryos showed altered mRNA splicing, including alternative splicing of various splicing factors and genes important for proper preimplantation embryonic development. Finally, we find that inhibition of tRFValCAC in zygotes delayed preimplantation embryonic development. Together, our results reveal a novel function of a sperm-enriched tRF in regulating alternating splicing and preimplantation embryonic development and shed light on the mechanism of sperm small RNA-mediated epigenetic inheritance.
精子中的小RNA与父本环境效应的代际表观遗传遗传有关;然而,它们的生物发生和功能仍知之甚少。我们之前鉴定出tRNA-缬氨酸-CAC-2(tRFValCAC)的5'片段是成熟精子中最丰富的小RNA之一。tRFValCAC在附睾睾丸后成熟过程中特异性地富集于精子中,并且我们发现它通过细胞外囊泡从附睾上皮细胞传递到精子。在这里,我们研究了tRFValCAC传递到精子的机制基础及其在早期胚胎中的功能。我们表明,tRFValCAC在附睾中与一种RNA结合蛋白,即不均一核核糖核蛋白A/B(hnRNPAB)相互作用,这种相互作用调节tRFValCAC分选和包装到细胞外囊泡中。在胚胎中,我们发现tRFValCAC调节早期胚胎mRNA的加工和剪接。在植入前胚胎中抑制tRFValCAC会改变参与RNA剪接和mRNA加工的基因的转录本丰度。重要的是,tRFValCAC抑制的胚胎表现出mRNA剪接改变,包括各种剪接因子和对植入前胚胎正常发育重要的基因的可变剪接。最后,我们发现合子中tRFValCAC的抑制会延迟植入前胚胎发育。总之,我们的结果揭示了一种富含精子的tRF在调节可变剪接和植入前胚胎发育方面的新功能,并阐明了精子小RNA介导的表观遗传遗传机制。