Wierzbicki Andrzej T, Ream Thomas S, Haag Jeremy R, Pikaard Craig S
Biology Department, Washington University, St. Louis, Missouri, USA.
Nat Genet. 2009 May;41(5):630-4. doi: 10.1038/ng.365. Epub 2009 Apr 19.
Retrotransposons and repetitive DNA elements in eukaryotes are silenced by small RNA-directed heterochromatin formation. In Arabidopsis, this process involves 24-nt siRNAs that bind to ARGONAUTE4 (AGO4) and facilitate the targeting of complementary loci via unknown mechanisms. Nuclear RNA polymerase V (Pol V) is an RNA silencing enzyme recently shown to generate noncoding transcripts at loci silenced by 24-nt siRNAs. We show that AGO4 physically interacts with these Pol V transcripts and is thereby recruited to the corresponding chromatin. We further show that DEFECTIVE IN MERISTEM SILENCING3 (DMS3), a structural maintenance of chromosomes (SMC) hinge-domain protein, functions in the assembly of Pol V transcription initiation or elongation complexes. Collectively, our data suggest that AGO4 is guided to target loci through base-pairing of associated siRNAs with nascent Pol V transcripts.
真核生物中的逆转座子和重复DNA元件通过小RNA介导的异染色质形成而沉默。在拟南芥中,这一过程涉及与AGO4结合的24个核苷酸的小干扰RNA(siRNAs),并通过未知机制促进对互补位点的靶向作用。核RNA聚合酶V(Pol V)是一种RNA沉默酶,最近发现它在被24个核苷酸的siRNAs沉默的位点上产生非编码转录本。我们发现AGO4与这些Pol V转录本发生物理相互作用,从而被招募到相应的染色质上。我们进一步表明,作为染色体结构维持(SMC)铰链结构域蛋白的分生组织沉默缺陷3(DMS3)在Pol V转录起始或延伸复合物的组装中发挥作用。总的来说,我们的数据表明,AGO4通过相关siRNAs与新生的Pol V转录本的碱基配对被引导至靶向位点。