Liu Chengxiu, Han Yuanyuan, Tong Pinfen, Kuang Dexuan, Li Na, Lu Caixia, Sun Xiaomei, Wang Wenguang, Dai Jiejie
The Center of Tree Shrew Germplasm Resources, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming, China.
Ann Transl Med. 2021 Apr;9(8):688. doi: 10.21037/atm-21-1293.
Breast intraductal papilloma (IP) is mainly caused by the abnormal proliferation of ductal epithelial cells. Tree shrews have potential as an animal model for the study of breast tumours; however, little is known regarding the transcriptome and DNA methylome landscapes of breast IP in tree shrews. In this research, we conducted whole-genome DNA methylation and transcriptome analyses of breast IP and normal mammary glands in tree shrews.
DNA methylation profiles were generated from the whole-genome bisulfite sequencing and whole-transcriptome landscapes of IP and control groups of tree shrews through strand-specific library construction and RNA sequencing. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes functional enrichment analyses and gene set enrichment analysis were performed. Spearman's correlation analysis was used to identify statistical relationships between gene expression and DNA methylation.
A genome-wide perspective of the epigenetic regulation of protein-coding genes in breast IP in tree shrews was obtained. The methylation levels at CG sites were considerably higher than those at CHG or CHH sites, and were highest in gene body regions. In total, 3,486, 82 and 361 differentially methylated regions (DMRs) were identified in the context of CG, CHG, and CHH, respectively, and 701 differentially methylated genes (DMGs) were found. Further, through transcriptomic analysis, 62 differentially expressed genes, 50 long noncoding RNAs, and 32 circular RNAs were identified in breast IP compared to normal mammary glands. Correlation analysis between the DNA methylation and transcriptome data revealed that 25 DMGs were also differentially expressed genes, among which the expression levels of 9 genes were negatively correlated with methylation levels in gene body regions. Importantly, integrated analysis identified 3 genes (PDZ domain-containing 1, ATPase plasma membrane Ca transporting 4 and Lymphocyte cytosolic protein 1) that could serve as candidates for further study of breast IP in tree shrews.
This research has unearthed the comprehensive landscape of the transcriptome and DNA methylome of spontaneous IP in tree shrews, as well as candidate tumorigenesis related genes in IP. These results will contribute to the use of tree shrews in animal models of breast tumours.
乳腺导管内乳头状瘤(IP)主要由导管上皮细胞异常增殖引起。树鼩有潜力作为研究乳腺肿瘤的动物模型;然而,关于树鼩乳腺IP的转录组和DNA甲基化组图谱知之甚少。在本研究中,我们对树鼩乳腺IP和正常乳腺进行了全基因组DNA甲基化和转录组分析。
通过链特异性文库构建和RNA测序,从树鼩IP组和对照组的全基因组亚硫酸氢盐测序及全转录组图谱中生成DNA甲基化谱。进行基因本体论和京都基因与基因组百科全书功能富集分析以及基因集富集分析。使用斯皮尔曼相关分析来确定基因表达与DNA甲基化之间的统计关系。
获得了树鼩乳腺IP中蛋白质编码基因表观遗传调控的全基因组视角。CG位点的甲基化水平明显高于CHG或CHH位点,且在基因体区域最高。总共在CG、CHG和CHH背景下分别鉴定出3486个、82个和361个差异甲基化区域(DMR),并发现701个差异甲基化基因(DMG)。此外,通过转录组分析,与正常乳腺相比,在乳腺IP中鉴定出62个差异表达基因、50个长链非编码RNA和32个环状RNA。DNA甲基化和转录组数据之间的相关性分析表明,25个DMG也是差异表达基因,其中9个基因的表达水平与基因体区域的甲基化水平呈负相关。重要的是,综合分析确定了3个基因(含PDZ结构域的1、质膜钙转运ATP酶4和淋巴细胞胞质蛋白1)可作为进一步研究树鼩乳腺IP的候选基因。
本研究揭示了树鼩自发性IP的转录组和DNA甲基化组的综合图谱,以及IP中与肿瘤发生相关的候选基因。这些结果将有助于树鼩在乳腺肿瘤动物模型中的应用。