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首页> 外文期刊>Plant Molecular Biology >Interplay among RNA polymerases II, IV and V in RNA-directed DNA methylation at a low copy transgene locus in Arabidopsis thaliana
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Interplay among RNA polymerases II, IV and V in RNA-directed DNA methylation at a low copy transgene locus in Arabidopsis thaliana

机译:RNA聚合酶II,IV和V在拟南芥低拷贝转基因基因座的RNA指导的DNA甲基化中的相互作用

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RNA-directed DNA methylation (RdDM) is an epigenetic process whereby small interfering RNAs (siRNAs) guide cytosine methylation of homologous DNA sequences. RdDM requires two specialized RNA polymerases: Pol IV transcribes the siRNA precursor whereas Pol V generates scaffold RNAs that interact with siRNAs and attract the methylation machinery. Recent evidence also suggests the involvement of RNA polymerase II (Pol II) in recruiting Pol IV and Pol V to low copy, intergenic loci. We demonstrated previously that Pol V-mediated methylation at a transgene locus in Arabidopsis spreads downstream of the originally targeted region by means of Pol IV/RNA-DEPENDENT RNA POLYMERASE2 (RDR2)-dependent 24-nt secondary siRNAs. Here we show that these secondary siRNAs can not only induce methylation in cis but also in trans at an unlinked target site, provided this sequence is transcribed by Pol II to produce a non-coding RNA. The Pol II transcript appears to be important for amplification of siRNAs at the unlinked target site because its presence correlates not only with methylation but also with elevated levels of 24-nt siRNAs. Potential target sites that lack an overlapping Pol II transcript and remain unmethylated in the presence of trans-acting 24-nt siRNAs can nevertheless acquire methylation in the presence of 21-24-nt hairpin-derived siRNAs, suggesting that RdDM of non-transcribed target sequences requires multiple size classes of siRNA. Our findings demonstrate that Pol II transcripts are not always needed for RdDM at low copy loci but they may intensify RdDM by facilitating amplification of Pol IV-dependent siRNAs at the DNA target site.
机译:RNA指导的DNA甲基化(RdDM)是一种表观遗传过程,其中小的干扰RNA(siRNA)指导同源DNA序列的胞嘧啶甲基化。 RdDM需要两种特殊的RNA聚合酶:Pol IV转录siRNA前体,而Pol V生成与siRNA相互作用并吸引甲基化机制的支架RNA。最近的证据还表明,RNA聚合酶II(Pol II)参与了将Pol IV和Pol V募集到低拷贝的基因间基因座。我们以前证明,在拟南芥属中一个转基因基因座上,Pol V介导的甲基化通过依赖于Pol IV / RNA依赖性RNA POLYMERASE2(RDR2)的24-nt二级siRNA扩散到最初的目标区域下游。在这里,我们显示这些次级siRNA不仅可以在顺式中诱导甲基化,而且可以在未连接的靶位点上反式诱导甲基化,前提是该序列被Pol II转录以产生非编码RNA。 Pol II转录本对于在未连接的靶位点扩增siRNA似乎很重要,因为它的存在不仅与甲基化相关,而且与24 nt siRNA的水平升高相关。缺少重叠的Pol II转录物且在反式作用的24-nt siRNA存在下仍未甲基化的潜在靶位点仍可在21-24 nt发夹衍生的siRNA存在下获得甲基化,这表明未转录靶标的RdDM序列需要多种大小的siRNA。我们的发现表明,低拷贝位点的RdDM并不总是需要Pol II转录本,但它们可能通过促进DNA靶点上依赖于Pol IV的siRNA的扩增而增强RdDM。

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