生物
增强子
西斯特
表观遗传学
DNA甲基化
遗传学
基因
表观遗传学
发起人
基因座(遗传学)
基因组
基因表达调控
基因表达
计算生物学
X-失活
X染色体
作者
Yaling Zhu,Zhimin Zhou,Tao Huang,Zhen Zhang,Wanbo Li,Ziqi Ling,Tao Jiang,Jiawen Yang,Siyu Yang,Yanyuan Xiao,Carole Charlier,Michel Georges,Bin Yang,Lusheng Huang
标识
DOI:10.1007/s11427-021-2034-5
摘要
The limited knowledge of genomic noncoding and regulatory regions has restricted our ability to decipher the genetic mechanisms underlying complex traits in pigs. In this study, we characterized the spatiotemporal landscape of putative enhancers and promoters and their target genes by combining H3K27ac-targeted ChIP-Seq and RNA-Seq in fetal (prenatal days 74-75) and adult (postnatal days 132-150) tissues (brain, liver, heart, muscle and small intestine) sampled from Asian aboriginal Bama Xiang and European highly selected Large White pigs of both sexes. We identified 101,290 H3K27ac peaks, marking 18,521 promoters and 82,769 enhancers, including peaks that were active across all tissues and developmental stages (which could indicate safe harbor locus for exogenous gene insertion) and tissue- and developmental stage-specific peaks (which regulate gene pathways matching tissue- and developmental stage-specific physiological functions). We found that H3K27ac and DNA methylation in the promoter region of the XIST gene may be involved in X chromosome inactivation and demonstrated the utility of the present resource for revealing the regulatory patterns of known causal genes and prioritizing candidate causal variants for complex traits in pigs. In addition, we identified an average of 1,124 super-enhancers per sample and found that they were more likely to show tissue-specific activity than ordinary peaks. We have developed a web browser to improve the accessibility of the results ( http://segtp.jxau.edu.cn/pencode/?genome=susScr11 ).
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