Lister Ryan, O'Malley Ronan C, Tonti-Filippini Julian, Gregory Brian D, Berry Charles C, Millar A Harvey, Ecker Joseph R
Plant Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
Cell. 2008 May 2;133(3):523-36. doi: 10.1016/j.cell.2008.03.029.
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 single-base 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, strand-specific mRNA-seq revealed altered transcript abundance of hundreds of genes, transposons, and unannotated intergenic transcripts upon modification of the DNA methylation state.
解读控制转录的多层表观遗传调控对于理解植物如何发育以及如何对环境做出反应至关重要。我们使用合成测序技术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)进行测序,以生成野生型拟南芥以及DNA甲基转移酶或去甲基酶活性缺陷型突变体的高度整合表观基因组图谱。在单碱基分辨率下,我们发现了广泛的、以前未检测到的DNA甲基化,确定了每个位点的甲基化背景和水平,并观察到局部序列对甲基化状态的影响。对小RNA的深度测序揭示了小RNA的位置与DNA甲基化之间的直接关系、CpG DNA甲基化缺失时小RNA生物合成的扰动,以及小RNA在RNA-DNA同源区域指导链特异性DNA甲基化的趋势。最后,链特异性mRNA-seq揭示了DNA甲基化状态改变后数百个基因、转座子和未注释的基因间转录本的转录本丰度发生了变化。