Kim John K, Gabel Harrison W, Kamath Ravi S, Tewari Muneesh, Pasquinelli Amy, Rual Jean-François, Kennedy Scott, Dybbs Michael, Bertin Nicolas, Kaplan Joshua M, Vidal Marc, Ruvkun Gary
Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Science. 2005 May 20;308(5725):1164-7. doi: 10.1126/science.1109267. Epub 2005 Mar 24.
RNA interference (RNAi) of target genes is triggered by double-stranded RNAs (dsRNAs) processed by conserved nucleases and accessory factors. To identify the genetic components required for RNAi, we performed a genome-wide screen using an engineered RNAi sensor strain of Caenorhabditis elegans. The RNAi screen identified 90 genes. These included Piwi/PAZ proteins, DEAH helicases, RNA binding/processing factors, chromatin-associated factors, DNA recombination proteins, nuclear import/export factors, and 11 known components of the RNAi machinery. We demonstrate that some of these genes are also required for germline and somatic transgene silencing. Moreover, the physical interactions among these potential RNAi factors suggest links to other RNA-dependent gene regulatory pathways.
靶基因的RNA干扰(RNAi)由保守核酸酶和辅助因子加工的双链RNA(dsRNA)触发。为了鉴定RNAi所需的遗传成分,我们使用工程化的秀丽隐杆线虫RNAi传感器菌株进行了全基因组筛选。RNAi筛选鉴定出90个基因。这些基因包括Piwi/PAZ蛋白、DEAH解旋酶、RNA结合/加工因子、染色质相关因子、DNA重组蛋白、核输入/输出因子以及RNAi机制的11个已知成分。我们证明,这些基因中的一些对于生殖系和体细胞转基因沉默也是必需的。此外,这些潜在RNAi因子之间的物理相互作用表明它们与其他RNA依赖性基因调控途径存在联系。