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Highly integrated single-base resolution maps of the epigenome in Arabidopsis

机译:拟南芥表观基因组的高度集成的单碱基分辨率图

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Deciphering the multiple layers of epigenetic regulation that control transcription is critical to understanding how plants develop and respond to their environment. Using sequencing-by-synthesis technology we directly sequenced the cytosine methylome (methylC-seq), transcriptome (mRNA-seq), and small RNA transcriptome (smRNA-seq) to generate highly integrated epigenome maps for wild-type Arabidopsis thaliana and mutants defective in DNA methyltransferase or demethylase activity. At singlebase resolution we discovered extensive, previously undetected DNA methylation, identified the context and level of methylation at each site, and observed local sequence effects upon methylation state. Deep sequencing of smRNAs revealed a direct relationship between the location of smRNAs and DNA methylation, perturbation of smRNA biogenesis upon loss of CpG DNA methylation, and a tendency for smRNAs to direct strand-specific DNA methylation in regions of RNA-DNA homology. Finally, strandspecific mRNA-seq revealed altered transcript abundance of hundreds of genes, transposons, and unannotated intergenic transcripts upon modification of the DNA methylation state.
机译:解读控制转录的表观遗传调控的多层结构对于理解植物如何发育以及对环境的反应至关重要。使用合成测序技术,我们直接对胞嘧啶甲基化组(methylC-seq),转录组(mRNA-seq)和小RNA转录组(smRNA-seq)进行了测序,以生成高度整合的表观基因组图谱,用于野生型拟南芥和缺陷型突变体在DNA甲基转移酶或脱甲基酶的活性。在单碱基分辨率下,我们发现了以前从未发现的广泛的DNA甲基化,鉴定了每个位点的甲基化背景和水平,并观察了局部序列对甲基化状态的影响。 smRNA的深度测序揭示了smRNA的位置与DNA甲基化,失去CpG DNA甲基化后smRNA生物发生的扰动以及smRNA在RNA-DNA同源区域中指导链特异性DNA甲基化的趋势之间存在直接关系。最后,链特异性mRNA-seq揭示了DNA甲基化状态修饰后数百种基因,转座子和未注释的基因间转录物的转录物丰度发生了变化。

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