Structure and sequence evolution in the pennycress ( Thlaspi arvense ) pangenome

IF 8.7 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2026-04-03 DOI:10.1111/nph.71111
Kevin A. Bird, Joanna L. Rifkin, Chloee M. McLaughlin, Avril M. Harder, Pawan Basnet, Ella Katz, Tomáš Brůna, Kerrie Barry, LoriBeth Boston, Christopher Daum, Jie Guo, Anna Lipzen, Christopher Plott, Jerry W. Jenkins, Rachel Walstead, Shanmugam Rajasekar, Jayson Talag, Katherine Frels, Kathleen Greenham, Shelby Ellison, Jane Grimwood, Jeremy Schmutz, Patrick P. Edger, J. Chris Pires, John T. Lovell, Daniel J. Kliebenstein
{"title":"Structure and sequence evolution in the pennycress ( Thlaspi arvense ) pangenome","authors":"Kevin A. Bird, Joanna L. Rifkin, Chloee M. McLaughlin, Avril M. Harder, Pawan Basnet, Ella Katz, Tomáš Brůna, Kerrie Barry, LoriBeth Boston, Christopher Daum, Jie Guo, Anna Lipzen, Christopher Plott, Jerry W. Jenkins, Rachel Walstead, Shanmugam Rajasekar, Jayson Talag, Katherine Frels, Kathleen Greenham, Shelby Ellison, Jane Grimwood, Jeremy Schmutz, Patrick P. Edger, J. Chris Pires, John T. Lovell, Daniel J. Kliebenstein","doi":"10.1111/nph.71111","DOIUrl":null,"url":null,"abstract":"Summary <jats:list list-type=\"bullet\"> <jats:list-item> Eukaryotic genomes harbor many forms of variation, including nucleotide diversity and structural polymorphisms, which experience natural selection and contribute to genome evolution and biodiversity. Harnessing this variation for agriculture hinges on our ability to detect, quantify, catalog, and deploy genetic diversity. </jats:list-item> <jats:list-item> Here, we explore seven complete genomes of the emerging biofuel crop pennycress ( <jats:italic>Thlaspi arvense</jats:italic> ) drawn from across the species' current genetic diversity to catalog variation in genome structure and content. </jats:list-item> <jats:list-item> Across this new pangenome resource, we find contrasting evolutionary modes in different genomic zones. Gene‐poor, repeat‐rich pericentromeric regions experience frequent rearrangements, including repeated centromere repositioning. By contrast, conserved gene‐dense chromosome arms maintain large‐scale synteny across accessions even in fast‐evolving NOD‐like receptor immune genes, where microsynteny breaks down across species, but gene cluster positioning macrosynteny is maintained. </jats:list-item> <jats:list-item> Our findings highlight that multiple elements of the genome experience dynamic evolution that conserves functional content on the chromosome scale but allows repositioning and presence–absence variation on a local scale. This diversity is invisible to classical reference‐based strategies and highlights the strength and utility of pangenomic resources. These results provide a valuable case study of rapid genomic structural evolution within a species and powerful resources for crop development in an emerging biofuel crop. </jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"420 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2026-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.71111","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Summary Eukaryotic genomes harbor many forms of variation, including nucleotide diversity and structural polymorphisms, which experience natural selection and contribute to genome evolution and biodiversity. Harnessing this variation for agriculture hinges on our ability to detect, quantify, catalog, and deploy genetic diversity. Here, we explore seven complete genomes of the emerging biofuel crop pennycress ( Thlaspi arvense ) drawn from across the species' current genetic diversity to catalog variation in genome structure and content. Across this new pangenome resource, we find contrasting evolutionary modes in different genomic zones. Gene‐poor, repeat‐rich pericentromeric regions experience frequent rearrangements, including repeated centromere repositioning. By contrast, conserved gene‐dense chromosome arms maintain large‐scale synteny across accessions even in fast‐evolving NOD‐like receptor immune genes, where microsynteny breaks down across species, but gene cluster positioning macrosynteny is maintained. Our findings highlight that multiple elements of the genome experience dynamic evolution that conserves functional content on the chromosome scale but allows repositioning and presence–absence variation on a local scale. This diversity is invisible to classical reference‐based strategies and highlights the strength and utility of pangenomic resources. These results provide a valuable case study of rapid genomic structural evolution within a species and powerful resources for crop development in an emerging biofuel crop.
pennycrea (Thlaspi arvense)泛基因组结构与序列演化
真核生物基因组包含多种形式的变异,包括核苷酸多样性和结构多态性,这些变异经历了自然选择,并有助于基因组进化和生物多样性。在农业中利用这种变异取决于我们检测、量化、分类和利用遗传多样性的能力。在这里,我们探索了新兴生物燃料作物pennycrese (Thlaspi arvense)的七个完整基因组,这些基因组来自该物种当前的遗传多样性,以编目基因组结构和内容的变化。在这个新的泛基因组资源中,我们在不同的基因组区发现了对比的进化模式。基因贫乏、重复序列丰富的中心点周围区域经历频繁的重排,包括重复的着丝粒重新定位。相比之下,即使在快速进化的NOD样受体免疫基因中,保守的基因密集染色体臂也能维持大范围的同质性,其中微同质性在物种间被破坏,但基因簇定位的宏观同质性得以维持。我们的研究结果强调,基因组的多个元素经历动态进化,在染色体尺度上保存功能内容,但在局部尺度上允许重新定位和存在-缺失变化。这种多样性在经典的基于参考的策略中是不可见的,并突出了泛基因组资源的优势和效用。这些结果为物种基因组结构的快速进化提供了有价值的研究案例,并为新兴生物燃料作物的作物开发提供了有力的资源。
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 求助全文
来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
×
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:604180095
Book学术官方微信
小红书