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利用甲基化C测序技术研究两个遗传背景不同的鸡品系的全基因组DNA甲基化组变异

Genome-wide DNA methylome variation in two genetically distinct chicken lines using MethylC-seq.

作者信息

Li Jinxiu, Li Rujiao, Wang Ying, Hu Xiaoxiang, Zhao Yiqiang, Li Li, Feng Chungang, Gu Xiaorong, Liang Fang, Lamont Susan J, Hu Songnian, Zhou Huaijun, Li Ning

机构信息

The State Key Laboratory for Agro-biotechnology, China Agricultural University, Beijing, 100193, China.

CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.

出版信息

BMC Genomics. 2015 Oct 23;16:851. doi: 10.1186/s12864-015-2098-8.

Abstract

BACKGROUND

DNA cytosine methylation is an important epigenetic modification that has significant effects on a variety of biological processes in animals. Avian species hold a crucial position in evolutionary history. In this study, we used whole-genome bisulfite sequencing (MethylC-seq) to generate single base methylation profiles of lungs in two genetically distinct and highly inbred chicken lines (Fayoumi and Leghorn) that differ in genetic resistance to multiple pathogens, and we explored the potential regulatory role of DNA methylation associated with immune response differences between the two chicken lines.

METHODS

The MethylC-seq was used to generate single base DNA methylation profiles of Fayoumi and Leghorn birds. In addition, transcriptome profiling using RNA-seq from the same chickens and tissues were obtained to interrogate how DNA methylation regulates gene transcription on a genome-wide scale.

RESULTS

The general DNA methylation pattern across different regions of genes was conserved compared to other species except for hyper-methylation of repeat elements, which was not observed in chicken. The methylation level of miRNA and pseudogene promoters was high, which indicates that silencing of these genes may be partially due to promoter hyper-methylation. Interestingly, the promoter regions of more recently evolved genes tended to be more highly methylated, whereas the gene body regions of evolutionarily conserved genes were more highly methylated than those of more recently evolved genes. Immune-related GO (Gene Ontology) terms were significantly enriched from genes within the differentially methylated regions (DMR) between Fayoumi and Leghorn, which implicates DNA methylation as one of the regulatory mechanisms modulating immune response differences between these lines.

CONCLUSIONS

This study establishes a single-base resolution DNA methylation profile of chicken lung and suggests a regulatory role of DNA methylation in controlling gene expression and maintaining genome transcription stability. Furthermore, profiling the DNA methylomes of two genetic lines that differ in disease resistance provides a unique opportunity to investigate the potential role of DNA methylation in host disease resistance. Our study provides a foundation for future studies on epigenetic modulation of host immune response to pathogens in chickens.

摘要

背景

DNA胞嘧啶甲基化是一种重要的表观遗传修饰,对动物的多种生物学过程具有显著影响。鸟类在进化史上占据关键地位。在本研究中,我们使用全基因组亚硫酸氢盐测序(MethylC-seq)来生成两种遗传上不同且高度近交的鸡品系(法尤米鸡和来航鸡)肺组织的单碱基甲基化图谱,这两个品系对多种病原体的遗传抗性不同,并且我们探讨了与这两个鸡品系免疫反应差异相关的DNA甲基化的潜在调控作用。

方法

使用MethylC-seq生成法尤米鸡和来航鸡的单碱基DNA甲基化图谱。此外,利用来自相同鸡只和组织的RNA-seq进行转录组分析,以研究DNA甲基化如何在全基因组范围内调控基因转录。

结果

与其他物种相比,基因不同区域总的DNA甲基化模式是保守的,但重复元件的高甲基化在鸡中未观察到。miRNA和假基因启动子的甲基化水平较高,这表明这些基因的沉默可能部分归因于启动子高甲基化。有趣的是,较新进化基因的启动子区域往往甲基化程度更高,而进化保守基因的基因体区域比新进化基因的甲基化程度更高。法尤米鸡和来航鸡之间差异甲基化区域(DMR)内的基因显著富集免疫相关的基因本体(GO)术语,这表明DNA甲基化是调节这两个品系免疫反应差异的调控机制之一。

结论

本研究建立了鸡肺的单碱基分辨率DNA甲基化图谱,并表明DNA甲基化在控制基因表达和维持基因组转录稳定性方面具有调控作用。此外,对两个抗病性不同的遗传品系进行DNA甲基化组分析,为研究DNA甲基化在宿主抗病性中的潜在作用提供了独特机会。我们的研究为未来关于鸡宿主对病原体免疫反应的表观遗传调控研究奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af46/4619007/e49c756a1cdc/12864_2015_2098_Fig1_HTML.jpg

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