Aluru Neelakanteswar, Karchner Sibel I, Krick Keegan S, Zhu Wei, Liu Jiang
Department of Biology, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA.
CAS Key Laboratory of Genomic Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, CAS, Beijing 100101, China.
Environ Epigenet. 2018 Apr 13;4(1):dvy005. doi: 10.1093/eep/dvy005. eCollection 2018 Jan.
There is growing evidence that environmental toxicants can affect various physiological processes by altering DNA methylation patterns. However, very little is known about the impact of toxicant-induced DNA methylation changes on gene expression patterns. The objective of this study was to determine the genome-wide changes in DNA methylation concomitant with altered gene expression patterns in response to 3, 3', 4, 4', 5-pentachlorobiphenyl (PCB126) exposure. We used PCB126 as a model environmental chemical because the mechanism of action is well-characterized, involving activation of aryl hydrocarbon receptor, a ligand-activated transcription factor. Adult zebrafish were exposed to 10 nM PCB126 for 24 h (water-borne exposure) and brain and liver tissues were sampled at 7 days post-exposure in order to capture both primary and secondary changes in DNA methylation and gene expression. We used enhanced Reduced Representation Bisulfite Sequencing and RNAseq to quantify DNA methylation and gene expression, respectively. Enhanced reduced representation bisulfite sequencing analysis revealed 573 and 481 differentially methylated regions in the liver and brain, respectively. Most of the differentially methylated regions are located more than 10 kilobases upstream of transcriptional start sites of the nearest neighboring genes. Gene Ontology analysis of these genes showed that they belong to diverse physiological pathways including development, metabolic processes and regeneration. RNAseq results revealed differential expression of genes related to xenobiotic metabolism, oxidative stress and energy metabolism in response to polychlorinated biphenyl exposure. There was very little correlation between differentially methylated regions and differentially expressed genes suggesting that the relationship between methylation and gene expression is dynamic and complex, involving multiple layers of regulation.
越来越多的证据表明,环境毒物可通过改变DNA甲基化模式影响各种生理过程。然而,关于毒物诱导的DNA甲基化变化对基因表达模式的影响却知之甚少。本研究的目的是确定在暴露于3,3',4,4',5-五氯联苯(PCB126)时,伴随基因表达模式改变的全基因组DNA甲基化变化。我们使用PCB126作为环境化学物质模型,因为其作用机制已得到充分表征,涉及芳烃受体(一种配体激活的转录因子)的激活。成年斑马鱼暴露于10 nM的PCB126中24小时(水体暴露),并在暴露后7天采集脑和肝组织样本,以捕捉DNA甲基化和基因表达的初级和次级变化。我们分别使用增强型简化代表性亚硫酸氢盐测序和RNA测序来量化DNA甲基化和基因表达。增强型简化代表性亚硫酸氢盐测序分析显示,肝脏和脑中分别有573个和481个差异甲基化区域。大多数差异甲基化区域位于最近邻基因转录起始位点上游10千碱基以上。对这些基因的基因本体分析表明,它们属于不同的生理途径,包括发育、代谢过程和再生。RNA测序结果显示,在多氯联苯暴露后,与异源物代谢、氧化应激和能量代谢相关的基因表达存在差异。差异甲基化区域与差异表达基因之间的相关性很小,这表明甲基化与基因表达之间的关系是动态且复杂的,涉及多层调控。