Wen Jiayu, Duan Hong, Bejarano Fernando, Okamura Katsutomo, Fabian Lacramioara, Brill Julie A, Bortolamiol-Becet Diane, Martin Raquel, Ruby J Graham, Lai Eric C
Sloan-Kettering Institute, Department of Developmental Biology, 1275 York Ave, Box 252, New York, NY 10065, USA.
Cell Biology Program, The Hospital for Sick Children, PGCRL, 686 Bay Street, Room 15.9716, Toronto, ON M5G 0A4, Canada.
Mol Cell. 2015 Jan 8;57(1):165-78. doi: 10.1016/j.molcel.2014.11.025. Epub 2014 Dec 24.
Although endogenous siRNAs (endo-siRNAs) have been described in many species, still little is known about their endogenous utility. Here, we show that Drosophila hairpin RNAs (hpRNAs) generate an endo-siRNA class with predominant expression in testes. Although hpRNAs are universally recently evolved, we identify highly complementary protein-coding targets for all hpRNAs. Importantly, we find broad evidence for evolutionary divergences that preferentially maintain compensatory pairing between hpRNAs and targets, serving as first evidence for adaptive selection for siRNA-mediated target regulation in metazoans. We demonstrate organismal impact of hpRNA activity, since knockout of hpRNA1 derepresses its target ATP synthase-β in testes and compromises spermatogenesis and male fertility. Moreover, we reveal surprising male-specific impact of RNAi factors on germ cell development and fertility, consistent with testis-directed function of the hpRNA pathway. Finally, the collected hpRNA loci chronicle an evolutionary timeline that reflects their origins from prospective target genes, mirroring a strategy described for plant miRNAs.
尽管在许多物种中都已描述了内源性小干扰RNA(endo-siRNA),但其内源性作用仍知之甚少。在此,我们表明果蝇发夹RNA(hpRNA)产生了一类在睾丸中占主导表达的endo-siRNA。尽管hpRNA最近普遍进化,但我们为所有hpRNA鉴定出了高度互补的蛋白质编码靶标。重要的是,我们发现了广泛的进化差异证据,这些差异优先维持hpRNA与靶标之间的补偿性配对,这是后生动物中siRNA介导的靶标调控适应性选择的首个证据。我们证明了hpRNA活性对生物体的影响,因为敲除hpRNA1会在睾丸中解除对其靶标ATP合酶-β的抑制,并损害精子发生和雄性生育力。此外,我们揭示了RNAi因子对生殖细胞发育和生育力具有惊人的雄性特异性影响,这与hpRNA途径的睾丸定向功能一致。最后,收集到的hpRNA基因座记录了一个进化时间线,反映了它们源自预期靶基因的起源,这与植物miRNA所描述的策略相似。