Ministry of Education Key Laboratory for Membraneless Organelles & Cellular Dynamics, Hefei National Laboratory for Physical Sciences at the Microscale, School of Life Sciences, Department of Obstetrics and Gynecology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, P.R. China.
CAS Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Hefei, Anhui 230027, P.R. China.
Nucleic Acids Res. 2021 Sep 20;49(16):9194-9210. doi: 10.1093/nar/gkab662.
Eukaryotic cells express a wide variety of endogenous small regulatory RNAs that function in the nucleus. We previously found that erroneous rRNAs induce the generation of antisense ribosomal siRNAs (risiRNAs) which silence the expression of rRNAs via the nuclear RNAi defective (Nrde) pathway. To further understand the biological roles and mechanisms of this class of small regulatory RNAs, we conducted forward genetic screening to identify factors involved in risiRNA generation in Caenorhabditis elegans. We found that risiRNAs accumulated in the RNA exosome mutants. risiRNAs directed the association of NRDE proteins with pre-rRNAs and the silencing of pre-rRNAs. In the presence of risiRNAs, NRDE-2 accumulated in the nucleolus and colocalized with RNA polymerase I. risiRNAs inhibited the transcription elongation of RNA polymerase I by decreasing RNAP I occupancy downstream of the RNAi-targeted site. Meanwhile, exosomes mislocalized from the nucleolus to nucleoplasm in suppressor of siRNA (susi) mutants, in which erroneous rRNAs accumulated. These results established a novel model of rRNA surveillance by combining ribonuclease-mediated RNA degradation with small RNA-directed nucleolar RNAi system.
真核细胞表达多种内源性的小分子调节 RNA,它们在细胞核中发挥作用。我们之前发现错误的 rRNA 诱导产生反义核糖体 siRNA(risiRNA),通过核 RNAi 缺陷(Nrde)途径沉默 rRNA 的表达。为了进一步了解这一类小分子调节 RNA 的生物学作用和机制,我们进行正向遗传筛选,以鉴定参与秀丽隐杆线虫 risiRNA 生成的因素。我们发现 risiRNA 在 RNA 外切酶突变体中积累。risiRNA 指导 NRDE 蛋白与 pre-rRNA 结合,并沉默 pre-rRNA。在 risiRNA 的存在下,NRDE-2 在核仁中积累,并与 RNA 聚合酶 I 共定位。risiRNA 通过降低 RNAi 靶向位点下游的 RNAP I 占有率来抑制 RNA 聚合酶 I 的转录延伸。同时,在错误的 rRNA 积累的抑制 siRNA(susi)突变体中,外切酶从核仁错误定位到核质。这些结果通过将核糖核酸酶介导的 RNA 降解与小分子 RNA 指导的核仁 RNAi 系统相结合,建立了 rRNA 监测的新模型。