Leopold Luciana E, Heestand Bree N, Seong Soobin, Shtessel Ludmila, Ahmed Shawn
Department of Genetics.
Department of Genetics, Lineberger Comprehensive Cancer Center, and.
Proc Natl Acad Sci U S A. 2015 May 19;112(20):E2667-76. doi: 10.1073/pnas.1501979112. Epub 2015 May 4.
Single-copy transgenes in Caenorhabditis elegans can be subjected to a potent, irreversible silencing process termed small RNA-induced epigenetic silencing (RNAe). RNAe is promoted by the Piwi Argonaute protein PRG-1 and associated Piwi-interacting RNAs (piRNAs), as well as by proteins that promote and respond to secondary small interfering RNA (siRNA) production. Here we define a related siRNA-mediated silencing process, termed "multigenerational RNAe," which can occur for transgenes that are maintained in a hemizygous state for several generations. We found that transgenes that contain either GFP or mCherry epitope tags can be silenced via multigenerational RNAe, whereas a transgene that possesses GFP and a perfect piRNA target site can be rapidly and permanently silenced via RNAe. Although previous studies have shown that PRG-1 is typically dispensable for maintenance of RNAe, we found that both initiation and maintenance of multigenerational RNAe requires PRG-1 and the secondary siRNA biogenesis protein RDE-2. Although silencing via RNAe is irreversible, we found that transgene expression can be restored when hemizygous transgenes that were silenced via multigenerational RNAe become homozygous. Furthermore, multigenerational RNAe was accelerated when meiotic pairing of the chromosome possessing the transgene was abolished. We propose that persistent lack of pairing during meiosis elicits a reversible multigenerational silencing response, which can lead to permanent transgene silencing. Multigenerational RNAe may be broadly relevant to single-copy transgenes used in experimental biology and to shaping the epigenomic landscape of diverse species, where genomic polymorphisms between homologous chromosomes commonly result in unpaired DNA during meiosis.
秀丽隐杆线虫中的单拷贝转基因可经历一种强大的、不可逆的沉默过程,称为小RNA诱导的表观遗传沉默(RNAe)。RNAe由Piwi Argonaute蛋白PRG-1和相关的Piwi相互作用RNA(piRNA)以及促进和响应二级小干扰RNA(siRNA)产生的蛋白质所促进。在这里,我们定义了一种相关的siRNA介导的沉默过程,称为“多代RNAe”,它可以发生在半合子状态下维持几代的转基因中。我们发现,含有GFP或mCherry表位标签的转基因可以通过多代RNAe沉默,而拥有GFP和完美piRNA靶位点的转基因可以通过RNAe快速且永久地沉默。尽管先前的研究表明PRG-1通常对于RNAe的维持是可有可无的,但我们发现多代RNAe的起始和维持都需要PRG-1和二级siRNA生物合成蛋白RDE-2。虽然通过RNAe的沉默是不可逆的,但我们发现,当通过多代RNAe沉默的半合子转基因变为纯合子时,转基因表达可以恢复。此外,当消除含有转基因的染色体的减数分裂配对时,多代RNAe会加速。我们提出,减数分裂过程中持续缺乏配对会引发一种可逆的多代沉默反应,这可能导致转基因的永久沉默。多代RNAe可能广泛适用于实验生物学中使用的单拷贝转基因,以及塑造不同物种的表观基因组景观,在这些物种中,同源染色体之间的基因组多态性通常会导致减数分裂期间未配对的DNA。