生物
DNA甲基化
RNA导向的DNA甲基化
表观遗传学
遗传学
表观基因组
染色质
照明菌甲基化试验
甲基化DNA免疫沉淀
亚硫酸氢盐测序
表观遗传学
组蛋白
计算生物学
拟南芥
核小体
拟南芥
差异甲基化区
基因组
甲基化
H3K4me3
基因
染色体构象捕获
细胞生物学
染色质重塑
基因表达
作者
Ryan Lister,Ronan C. O'Malley,Julian Tonti-Filippini,Brian D. Gregory,Charles C. Berry,A. Harvey Millar,Joseph R. Ecker
出处
期刊:Cell
[Cell Press]
日期:2008-05-02
卷期号:133 (3): 523-536
被引量:2067
标识
DOI:10.1016/j.cell.2008.03.029
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI