State Key Laboratory for Crop Genetics and Germplasm Enhancement, JiangSu Collaborative Innovation Center for Modern Crop Production, Nanjing Agricultural University, Nanjing, Jiangsu 210095, P.R. China.
School of Forest Resources and Environmental Science, Michigan Technological University, Houghton, Michigan 49931, USA.
Genome Res. 2019 Aug;29(8):1287-1297. doi: 10.1101/gr.246009.118. Epub 2019 Jul 1.
We conducted genome-wide identification of R-loops followed by integrative analyses of R-loops with relation to gene expression and epigenetic signatures in the rice genome. We found that the correlation between gene expression levels and profiled R-loop peak levels was dependent on the positions of R-loops within gene structures (hereafter named "genic position"). Both antisense only (ASO)-R-loops and sense/antisense (S/AS)-R-loops sharply peaked around transcription start sites (TSSs), and these peak levels corresponded positively with transcript levels of overlapping genes. In contrast, sense only (SO)-R-loops were generally spread over the coding regions, and their peak levels corresponded inversely to transcript levels of overlapping genes. In addition, integrative analyses of R-loop data with existing RNA-seq, chromatin immunoprecipitation sequencing (ChIP-seq), DNase I hypersensitive sites sequencing (DNase-seq), and whole-genome bisulfite sequencing (WGBS or BS-seq) data revealed interrelationships and intricate connections among R-loops, gene expression, and epigenetic signatures. Experimental validation provided evidence that the demethylation of both DNA and histone marks can influence R-loop peak levels on a genome-wide scale. This is the first study in plants that reveals novel functional aspects of R-loops, their interrelations with epigenetic methylation, and roles in transcriptional regulation.
我们对水稻基因组中的 R 环进行了全基因组鉴定,并对 R 环与基因表达和表观遗传特征的关系进行了综合分析。我们发现,基因表达水平与 R 环峰水平之间的相关性取决于 R 环在基因结构内的位置(以下称为“基因位置”)。反义仅(ASO)-R 环和正义/反义(S/AS)-R 环在转录起始位点(TSS)周围急剧上升,这些峰值水平与重叠基因的转录水平呈正相关。相比之下,正义仅(SO)-R 环通常分布在编码区,其峰值水平与重叠基因的转录水平呈负相关。此外,将 R 环数据与现有的 RNA-seq、染色质免疫沉淀测序(ChIP-seq)、DNase I 超敏位点测序(DNase-seq)和全基因组亚硫酸氢盐测序(WGBS 或 BS-seq)数据进行综合分析,揭示了 R 环、基因表达和表观遗传特征之间的相互关系和复杂联系。实验验证提供了证据表明,DNA 和组蛋白标记的去甲基化可以影响全基因组范围内的 R 环峰水平。这是在植物中首次揭示 R 环的新功能方面、它们与表观遗传甲基化的相互关系以及在转录调控中的作用。