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PNAS Plus: Caenorhabditis elegans RSD-2 and RSD-6 promote germ cell immortality by maintaining small interfering RNA populations

机译:PNAS Plus:秀丽隐杆线虫RSD-2和RSD-6通过维持少量干扰RNA种群来促进生殖细胞永生

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摘要

Germ cells are maintained in a pristine non-aging state as they proliferate over generations. Here, we show that a novel function of the Caenorhabditis elegans RNA interference proteins RNAi spreading defective (RSD)-2 and RSD-6 is to promote germ cell immortality at high temperature. rsd mutants cultured at high temperatures became progressively sterile and displayed loss of small interfering RNAs (siRNAs) that target spermatogenesis genes, simple repeats, and transposons. Desilencing of spermatogenesis genes occurred in late-generation rsd mutants, although defective spermatogenesis was insufficient to explain the majority of sterility. Increased expression of repetitive loci occurred in both germ and somatic cells of late-generation rsd mutant adults, suggesting that desilencing of many heterochromatic segments of the genome contributes to sterility. Nuclear RNAi defective (NRDE)-2 promotes nuclear silencing in response to exogenous double-stranded RNA, and our data imply that RSD-2, RSD-6, and NRDE-2 function in a common transgenerational nuclear silencing pathway that responds to endogenous siRNAs. We propose that RSD-2 and RSD-6 promote germ cell immortality at stressful temperatures by maintaining transgenerational epigenetic inheritance of endogenous siRNA populations that promote genome silencing.
机译:生殖细胞随着世代的繁殖而保持原始的非衰老状态。在这里,我们表明秀丽隐杆线虫RNA干扰蛋白RNAi传播缺陷(RSD)-2和RSD-6的一种新功能是在高温下促进生殖细胞的永生。在高温下培养的rsd突变体逐渐变得无菌,并显示出针对精子发生基因,简单重复序列和转座子的小干扰RNA(siRNA)的丢失。尽管有缺陷的精子发生不足以解释大多数不育现象,但在晚期rsd突变体中发生了精子发生基因的沉默。重复基因座的表达增加发生在后代rsd突变体成年人的生殖细胞和体细胞中,这表明基因组许多异色片段的沉默导致了不育。核RNAi缺陷(NRDE)-2响应外源双链RNA促进核沉默,我们的数据表明RSD-2,RSD-6和NRDE-2在对内源性siRNA响应的常见跨代核沉默途径中发挥作用。 。我们建议RSD-2和RSD-6通过维持促进基因组沉默的内源性siRNA群体的跨代表观遗传遗传来在压力温度下促进生殖细胞永生。

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