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Chromatin and siRNA pathways cooperate to maintain DNA methylation of small transposable elements in Arabidopsis.

机译:染色质和siRNA途径共同维持拟南芥中小转座因子的DNA甲基化。

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Background: DNA methylation occurs at preferred sites in eukaryotes. In Arabidopsis, DNA cytosine methylation is maintained by three subfamilies of methyltransferases with distinct substrate specificities and different modes of action. Targeting of cytosine methylation at selected loci has been found to sometimes involve histone H3 methylation and small interfering (si)RNAs. However, the relationship between different cytosine methylation pathways and their preferred targets is not known. Results: We used a microarray-based profiling method to explore the involvement of Arabidopsis CMT3 and DRM DNA methyltransferases, a histone H3 lysine-9 methyltransferase (KYP) and an Argonaute-related siRNA silencing component (AGO4) in methylating target loci. We found that KYP targets are also CMT3 targets, suggesting that histone methylation maintains CNG methylation genome-wide. CMT3 and KYP targets show similar proximal distributions that correspond to the overall distribution of transposable elements of all types, whereas DRM targets are distributed more distally along the chromosome. We find an inverse relationship between element size and loss of methylation in ago4 and drm mutants. Conclusion: We conclude that the targets of both DNA methylation and histone H3K9 methylation pathways are transposable elements genome-wide, irrespective of element type and position. Our findings also suggest that RNA-directed DNA methylation is required to silence isolated elements that may be too small to be maintained in a silent state by a chromatin-based mechanism alone. Thus, parallel pathways would be needed to maintain silencing of transposable elements..
机译:背景:DNA甲基化发生在真核生物的首选位点。在拟南芥中,DNA胞嘧啶甲基化由甲基转移酶的三个亚家族维持,它们具有不同的底物特异性和不同的作用方式。已经发现,胞嘧啶甲基化针对所选基因座有时会涉及组蛋白H3甲基化和小的干扰(si)RNA。然而,尚不清楚不同胞嘧啶甲基化途径与其优选靶标之间的关系。结果:我们使用基于微阵列的分析方法来探索拟南芥CMT3和DRM DNA甲基转移酶,组蛋白H3赖氨酸9甲基转移酶(KYP)和Argonaute相关的siRNA沉默组件(AGO4)在甲基化靶位点中的参与。我们发现KYP靶标也是CMT3靶标,表明组蛋白甲基化可在整个基因组范围内维持CNG甲基化。 CMT3和KYP靶标显示出相似的近端分布,对应于所有类型的转座因子的总体分布,而DRM靶标则沿染色体向远端分布。我们发现元件大小与ago4和drm突变体中的甲基化损失之间存在反比关系。结论:我们得出结论,DNA甲基化和组蛋白H3K9甲基化途径的靶标是全基因组范围内的可转座元件,而与元件类型和位置无关。我们的发现还表明,需要RNA定向的DNA甲基化来沉默分离的元件,这些元件可能很小,无法仅通过基于染色质的机制维持在沉默状态。因此,将需要平行的途径来维持转座元件的沉默。

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