High-quality sika deer omics data and integrative analysis reveal genic and cellular regulation of antler regeneration

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Genome research Pub Date : 2024-11-14 DOI:10.1101/gr.279448.124
Zihe Li, Ziyu Xu, Lei Zhu, Tao Qin, Jinrui Ma, Zhanying Feng, Huishan Yue, Qing Guan, Botong Zhou, Ge Han, Guokun Zhang, Chunyi Li, Shuaijun Jia, Qiang Qiu, Dingjun Hao, Yong Wang, Wen Wang
{"title":"High-quality sika deer omics data and integrative analysis reveal genic and cellular regulation of antler regeneration","authors":"Zihe Li, Ziyu Xu, Lei Zhu, Tao Qin, Jinrui Ma, Zhanying Feng, Huishan Yue, Qing Guan, Botong Zhou, Ge Han, Guokun Zhang, Chunyi Li, Shuaijun Jia, Qiang Qiu, Dingjun Hao, Yong Wang, Wen Wang","doi":"10.1101/gr.279448.124","DOIUrl":null,"url":null,"abstract":"Antler is the only organ that can fully regenerate annually in mammals. However, the regulatory pattern and mechanism of gene expression and cell differentiation during this process remain largely unknown. Here, we obtain comprehensive assembly and gene annotation of the sika deer (<em>Cervus nippon</em>) genome. Together with large-scale chromatin accessibility and gene expression data, we construct gene regulatory networks involved in antler regeneration, identifying four transcription factors, <em>MYC</em>, <em>KLF4</em>, <em>NFE2L2</em>, and <em>JDP2</em> with high regulatory activity across whole regeneration process. Comparative studies and luciferase reporter assay suggest the <em>MYC</em> expression driven by a cervid-specific regulatory element might be important for antler regenerative ability. We further develop a model called cTOP which integrates single-cell data with bulk regulatory networks and find <em>PRDM1</em>, <em>FOSL1</em>, <em>BACH1</em>, and <em>NFATC1</em> as potential pivotal factors in antler stem cell activation and osteogenic differentiation. Additionally, we uncover interactions within and between cell programs and pathways during the regeneration process. These findings provide insights into the gene and cell regulatory mechanisms of antler regeneration, particularly in stem cell activation and differentiation.","PeriodicalId":12678,"journal":{"name":"Genome research","volume":"22 1","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/gr.279448.124","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Antler is the only organ that can fully regenerate annually in mammals. However, the regulatory pattern and mechanism of gene expression and cell differentiation during this process remain largely unknown. Here, we obtain comprehensive assembly and gene annotation of the sika deer (Cervus nippon) genome. Together with large-scale chromatin accessibility and gene expression data, we construct gene regulatory networks involved in antler regeneration, identifying four transcription factors, MYC, KLF4, NFE2L2, and JDP2 with high regulatory activity across whole regeneration process. Comparative studies and luciferase reporter assay suggest the MYC expression driven by a cervid-specific regulatory element might be important for antler regenerative ability. We further develop a model called cTOP which integrates single-cell data with bulk regulatory networks and find PRDM1, FOSL1, BACH1, and NFATC1 as potential pivotal factors in antler stem cell activation and osteogenic differentiation. Additionally, we uncover interactions within and between cell programs and pathways during the regeneration process. These findings provide insights into the gene and cell regulatory mechanisms of antler regeneration, particularly in stem cell activation and differentiation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
高质量梅花鹿全息数据和综合分析揭示了鹿茸再生的基因和细胞调控机制
鹿角是哺乳动物中唯一能每年完全再生的器官。然而,这一过程中基因表达和细胞分化的调控模式和机制在很大程度上仍是未知的。在这里,我们获得了梅花鹿(Cervus nippon)基因组的全面组装和基因注释。结合大规模染色质可及性和基因表达数据,我们构建了参与鹿茸再生的基因调控网络,发现 MYC、KLF4、NFE2L2 和 JDP2 四个转录因子在整个再生过程中具有较高的调控活性。比较研究和荧光素酶报告实验表明,由鹿类特异性调控元件驱动的MYC表达可能对鹿茸的再生能力非常重要。我们进一步建立了一个名为 cTOP 的模型,该模型将单细胞数据与大体调控网络相结合,发现 PRDM1、FOSL1、BACH1 和 NFATC1 是鹿茸干细胞活化和成骨分化的潜在关键因素。此外,我们还发现了再生过程中细胞程序和途径内部和之间的相互作用。这些发现为鹿茸再生的基因和细胞调控机制,特别是干细胞活化和分化提供了深入的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Genome research
Genome research 生物-生化与分子生物学
CiteScore
12.40
自引率
1.40%
发文量
140
审稿时长
6 months
期刊介绍: Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine. Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies. New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.
期刊最新文献
Modeling gene interactions in polygenic prediction via geometric deep learning High-quality sika deer omics data and integrative analysis reveal genic and cellular regulation of antler regeneration ISWI1 complex proteins facilitate developmental genome editing in Paramecium Haplotype-resolved genome and population genomics of the threatened garden dormouse in Europe. Multisample motif discovery and visualization for tandem repeats
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1