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

被引:1794
作者
Lister, Ryan [1 ,2 ]
O'Malley, Ronan C. [1 ,2 ]
Tonti-Filippini, Julian
Gregory, Brian D. [1 ,2 ]
Berry, Charles C. [3 ]
Millar, A. Harvey [4 ]
Ecker, Joseph R. [1 ,2 ]
机构
[1] Salk Inst Biol Studies, Plant Biol Lab, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Genom Anal Lab, La Jolla, CA 92037 USA
[3] Univ Calif San Diego, Dept Family Prevent Med, La Jolla, CA 92093 USA
[4] Univ Western Australia, ARC Ctr Excellence Plant Energy Biol, Crawley, WA 6009, Australia
关键词
D O I
10.1016/j.cell.2008.03.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 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.
引用
收藏
页码:523 / 536
页数:14
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