DNA 甲基化和转录组分析揭示了三种猕猴的表观基因组差异

IF 3.5 2区 生物学 Q1 EVOLUTIONARY BIOLOGY
Jiao Wang, Xuyuan Liu, Yue Lan, Tengcheng Que, Jing Li, Bisong Yue, Zhenxin Fan
{"title":"DNA 甲基化和转录组分析揭示了三种猕猴的表观基因组差异","authors":"Jiao Wang,&nbsp;Xuyuan Liu,&nbsp;Yue Lan,&nbsp;Tengcheng Que,&nbsp;Jing Li,&nbsp;Bisong Yue,&nbsp;Zhenxin Fan","doi":"10.1111/eva.13604","DOIUrl":null,"url":null,"abstract":"<p>Macaques (genus <i>Macaca</i>) are the most widely distributed non-human primates, and their evolutionary history, gene expression profiles, and genetic differences have been extensively studied. However, the DNA methylomes of macaque species are not available in public databases, which hampers understanding of epigenetic differences among macaque species. Epigenetic modifications can potentially affect development, physiology, behavior, and evolution. Here, we investigated the methylation patterns of the Tibetan macaque (<i>M. thibetana</i>; TM), Chinese rhesus macaque (<i>M. mulatta lasiota</i>; CR), and crab-eating macaque (<i>M. fascicularis</i>; CE) through whole-genome bisulfite sequencing from peripheral blood. We compared genome-wide methylation site information for the three species. We identified 12,128 (CR vs. CE), 59,165 (CR vs. TM), and 39,751 (CE vs. TM) differentially methylated regions (DMRs) in the three macaques. Furthermore, we obtained the differentially expressed genes (DEGs) among the three macaque species. The differences between CR and CE were smaller at both the methylome and transcriptome levels than compared with TM (CR vs. TM and CE vs. TM). We also found a change in the density of single nucleotide mutations in DMRs relative to their flanking regions, indicating a potential mechanism through which genomic alterations may modulate methylation landscapes, thereby influencing the transcriptome. Functional enrichment analyses showed the DMR-related genes were enriched in developmental processes and neurological functions, such as the growth hormone-related pathway, insulin secretion pathway, thyroid hormone synthesis pathway, morphine addiction, and GABAergic synapses. These differences may be associated with variations in physiology and habitat among the macaques. Our study provides one of the first genome-wide comparisons of genetic, gene expression, and epigenetic variations across different macaques. Our results should facilitate further research on comparative genomic and genetic differences in macaque species.</p>","PeriodicalId":168,"journal":{"name":"Evolutionary Applications","volume":"17 2","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2023-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/eva.13604","citationCount":"0","resultStr":"{\"title\":\"DNA methylation and transcriptome analysis reveal epigenomic differences among three macaque species\",\"authors\":\"Jiao Wang,&nbsp;Xuyuan Liu,&nbsp;Yue Lan,&nbsp;Tengcheng Que,&nbsp;Jing Li,&nbsp;Bisong Yue,&nbsp;Zhenxin Fan\",\"doi\":\"10.1111/eva.13604\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Macaques (genus <i>Macaca</i>) are the most widely distributed non-human primates, and their evolutionary history, gene expression profiles, and genetic differences have been extensively studied. However, the DNA methylomes of macaque species are not available in public databases, which hampers understanding of epigenetic differences among macaque species. Epigenetic modifications can potentially affect development, physiology, behavior, and evolution. Here, we investigated the methylation patterns of the Tibetan macaque (<i>M. thibetana</i>; TM), Chinese rhesus macaque (<i>M. mulatta lasiota</i>; CR), and crab-eating macaque (<i>M. fascicularis</i>; CE) through whole-genome bisulfite sequencing from peripheral blood. We compared genome-wide methylation site information for the three species. We identified 12,128 (CR vs. CE), 59,165 (CR vs. TM), and 39,751 (CE vs. TM) differentially methylated regions (DMRs) in the three macaques. Furthermore, we obtained the differentially expressed genes (DEGs) among the three macaque species. The differences between CR and CE were smaller at both the methylome and transcriptome levels than compared with TM (CR vs. TM and CE vs. TM). We also found a change in the density of single nucleotide mutations in DMRs relative to their flanking regions, indicating a potential mechanism through which genomic alterations may modulate methylation landscapes, thereby influencing the transcriptome. Functional enrichment analyses showed the DMR-related genes were enriched in developmental processes and neurological functions, such as the growth hormone-related pathway, insulin secretion pathway, thyroid hormone synthesis pathway, morphine addiction, and GABAergic synapses. These differences may be associated with variations in physiology and habitat among the macaques. Our study provides one of the first genome-wide comparisons of genetic, gene expression, and epigenetic variations across different macaques. Our results should facilitate further research on comparative genomic and genetic differences in macaque species.</p>\",\"PeriodicalId\":168,\"journal\":{\"name\":\"Evolutionary Applications\",\"volume\":\"17 2\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2023-10-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/eva.13604\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolutionary Applications\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/eva.13604\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"EVOLUTIONARY BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolutionary Applications","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/eva.13604","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

猕猴(猕猴属)是分布最广的非人灵长类动物,它们的进化史、基因表达谱和遗传差异已被广泛研究。然而,猕猴物种的 DNA 甲基组尚未出现在公共数据库中,这阻碍了人们对猕猴物种间表观遗传差异的了解。表观遗传修饰可能会影响发育、生理、行为和进化。在这里,我们通过外周血全基因组亚硫酸氢盐测序研究了藏猕猴(M. thibetana; TM)、中国猕猴(M. mulatta lasiota; CR)和食蟹猕猴(M. fascicularis; CE)的甲基化模式。我们比较了这三个物种的全基因组甲基化位点信息。我们在三种猕猴中分别发现了 12,128 个(CR vs. CE)、59,165 个(CR vs. TM)和 39,751 个(CE vs. TM)差异甲基化区域(DMRs)。此外,我们还获得了三种猕猴的差异表达基因(DEGs)。与 TM 相比,CR 和 CE 在甲基组和转录组水平上的差异都较小(CR vs. TM 和 CE vs. TM)。我们还发现,相对于其侧翼区域,DMRs 中单核苷酸突变的密度发生了变化,这表明基因组改变可能通过一种潜在的机制改变甲基化景观,从而影响转录组。功能富集分析表明,DMR相关基因富集于发育过程和神经功能中,如生长激素相关途径、胰岛素分泌途径、甲状腺激素合成途径、吗啡成瘾和GABA能突触。这些差异可能与猕猴生理和栖息地的不同有关。我们的研究首次对不同猕猴的遗传、基因表达和表观遗传变异进行了全基因组比较。我们的研究结果将有助于进一步研究猕猴物种的比较基因组和遗传差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DNA methylation and transcriptome analysis reveal epigenomic differences among three macaque species

DNA methylation and transcriptome analysis reveal epigenomic differences among three macaque species

Macaques (genus Macaca) are the most widely distributed non-human primates, and their evolutionary history, gene expression profiles, and genetic differences have been extensively studied. However, the DNA methylomes of macaque species are not available in public databases, which hampers understanding of epigenetic differences among macaque species. Epigenetic modifications can potentially affect development, physiology, behavior, and evolution. Here, we investigated the methylation patterns of the Tibetan macaque (M. thibetana; TM), Chinese rhesus macaque (M. mulatta lasiota; CR), and crab-eating macaque (M. fascicularis; CE) through whole-genome bisulfite sequencing from peripheral blood. We compared genome-wide methylation site information for the three species. We identified 12,128 (CR vs. CE), 59,165 (CR vs. TM), and 39,751 (CE vs. TM) differentially methylated regions (DMRs) in the three macaques. Furthermore, we obtained the differentially expressed genes (DEGs) among the three macaque species. The differences between CR and CE were smaller at both the methylome and transcriptome levels than compared with TM (CR vs. TM and CE vs. TM). We also found a change in the density of single nucleotide mutations in DMRs relative to their flanking regions, indicating a potential mechanism through which genomic alterations may modulate methylation landscapes, thereby influencing the transcriptome. Functional enrichment analyses showed the DMR-related genes were enriched in developmental processes and neurological functions, such as the growth hormone-related pathway, insulin secretion pathway, thyroid hormone synthesis pathway, morphine addiction, and GABAergic synapses. These differences may be associated with variations in physiology and habitat among the macaques. Our study provides one of the first genome-wide comparisons of genetic, gene expression, and epigenetic variations across different macaques. Our results should facilitate further research on comparative genomic and genetic differences in macaque species.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Evolutionary Applications
Evolutionary Applications 生物-进化生物学
CiteScore
8.50
自引率
7.30%
发文量
175
审稿时长
6 months
期刊介绍: Evolutionary Applications is a fully peer reviewed open access journal. It publishes papers that utilize concepts from evolutionary biology to address biological questions of health, social and economic relevance. Papers are expected to employ evolutionary concepts or methods to make contributions to areas such as (but not limited to): medicine, agriculture, forestry, exploitation and management (fisheries and wildlife), aquaculture, conservation biology, environmental sciences (including climate change and invasion biology), microbiology, and toxicology. All taxonomic groups are covered from microbes, fungi, plants and animals. In order to better serve the community, we also now strongly encourage submissions of papers making use of modern molecular and genetic methods (population and functional genomics, transcriptomics, proteomics, epigenetics, quantitative genetics, association and linkage mapping) to address important questions in any of these disciplines and in an applied evolutionary framework. Theoretical, empirical, synthesis or perspective papers are welcome.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信