• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

有毒植物属(,十字花科)中祖先防御和新防御的独立进化。

Independent evolution of ancestral and novel defenses in a genus of toxic plants (, Brassicaceae).

机构信息

Institute of Plant Sciences, University of Bern, Bern, Switzerland.

Boyce Thompson Institute, Ithaca, United States.

出版信息

Elife. 2020 Apr 7;9:e51712. doi: 10.7554/eLife.51712.

DOI:10.7554/eLife.51712
PMID:32252891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7180059/
Abstract

Phytochemical diversity is thought to result from coevolutionary cycles as specialization in herbivores imposes diversifying selection on plant chemical defenses. Plants in the speciose genus (Brassicaceae) produce both ancestral glucosinolates and evolutionarily novel cardenolides as defenses. Here we test macroevolutionary hypotheses on co-expression, co-regulation, and diversification of these potentially redundant defenses across this genus. We sequenced and assembled the genome of and foliar transcriptomes of 47 additional species to construct a phylogeny from 9868 orthologous genes, revealing several geographic clades but also high levels of gene discordance. Concentrations, inducibility, and diversity of the two defenses varied independently among species, with no evidence for trade-offs. Closely related, geographically co-occurring species shared similar cardenolide traits, but not glucosinolate traits, likely as a result of specific selective pressures acting on each defense. Ancestral and novel chemical defenses in thus appear to provide complementary rather than redundant functions.

摘要

植物化学多样性被认为是协同进化循环的结果,因为草食动物的特化对植物的化学防御施加了多样化选择。在物种丰富的 属(十字花科)中,植物既产生原始的硫代葡萄糖苷,也产生进化上新颖的卡烯内酯作为防御。在这里,我们测试了这些潜在冗余防御在协同表达、协同调控和多样化方面的宏观进化假设。我们对 进行了测序和组装,并对 47 个附加 物种的叶片转录组进行了测序,构建了一个来自 9868 个直系同源基因的系统发育树,揭示了几个地理分支,但也存在高水平的基因不一致性。两种防御物质的浓度、诱导性和多样性在物种间独立变化,没有证据表明存在权衡。密切相关的、地理上共存的物种具有相似的卡烯内酯特征,但没有硫代葡萄糖苷特征,这可能是由于每种防御物质受到特定的选择性压力。因此, 中的祖先和新的化学防御似乎提供了互补而不是冗余的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/e336793d3c1a/elife-51712-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/30e889d1541c/elife-51712-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/93464fb4a67a/elife-51712-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/dc8679a26e45/elife-51712-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/8cbcd75062a8/elife-51712-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/558285a7e107/elife-51712-fig2-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/3fc0b20b4d7a/elife-51712-fig2-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/504d39d56f36/elife-51712-fig2-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/2ae62b7fffce/elife-51712-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/27444564cdcb/elife-51712-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/38d7569cdc3e/elife-51712-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/4b203f86e5a4/elife-51712-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/48406f131b4c/elife-51712-fig3-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/2ad997d24e4b/elife-51712-fig3-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/e594aec6b3be/elife-51712-fig3-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/2d6f0e96b2e9/elife-51712-fig3-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/031d6695d7cb/elife-51712-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/9e826d3f3b88/elife-51712-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/0bcdeeadff3e/elife-51712-fig4-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/be68632fe71f/elife-51712-fig4-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/9b973238631d/elife-51712-fig4-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/12d99067394e/elife-51712-fig4-figsupp9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/71ed98871e6e/elife-51712-fig4-figsupp11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/e336793d3c1a/elife-51712-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/30e889d1541c/elife-51712-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/93464fb4a67a/elife-51712-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/dc8679a26e45/elife-51712-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/8cbcd75062a8/elife-51712-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/558285a7e107/elife-51712-fig2-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/3fc0b20b4d7a/elife-51712-fig2-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/504d39d56f36/elife-51712-fig2-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/2ae62b7fffce/elife-51712-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/27444564cdcb/elife-51712-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/38d7569cdc3e/elife-51712-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/4b203f86e5a4/elife-51712-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/48406f131b4c/elife-51712-fig3-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/2ad997d24e4b/elife-51712-fig3-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/e594aec6b3be/elife-51712-fig3-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/2d6f0e96b2e9/elife-51712-fig3-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/031d6695d7cb/elife-51712-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/9e826d3f3b88/elife-51712-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/0bcdeeadff3e/elife-51712-fig4-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/be68632fe71f/elife-51712-fig4-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/9b973238631d/elife-51712-fig4-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/12d99067394e/elife-51712-fig4-figsupp9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/71ed98871e6e/elife-51712-fig4-figsupp11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7180059/e336793d3c1a/elife-51712-fig5.jpg

相似文献

1
Independent evolution of ancestral and novel defenses in a genus of toxic plants (, Brassicaceae).有毒植物属(,十字花科)中祖先防御和新防御的独立进化。
Elife. 2020 Apr 7;9:e51712. doi: 10.7554/eLife.51712.
2
Less Is More: a Mutation in the Chemical Defense Pathway of Erysimum cheiranthoides (Brassicaceae) Reduces Total Cardenolide Abundance but Increases Resistance to Insect Herbivores.少即是多:欧洲桂竹香(十字花科)化学防御途径中的一个突变降低了总强心苷的丰度,但增加了对昆虫食草动物的抗性。
J Chem Ecol. 2020 Dec;46(11-12):1131-1143. doi: 10.1007/s10886-020-01225-y. Epub 2020 Nov 12.
3
Acropetal and basipetal cardenolide transport in Erysimum cheiranthoides (wormseed wallflower).鹤虱属(wormseed wallflower)植物沿茎由上至下和由下至上的强心甾内酯类化合物的运输。
Phytochemistry. 2021 Dec;192:112965. doi: 10.1016/j.phytochem.2021.112965. Epub 2021 Oct 2.
4
Four enzymes control natural variation in the steroid core of cardenolides.四种酶控制着强心苷甾体核心结构的自然变异。
bioRxiv. 2024 Apr 11:2024.04.10.588904. doi: 10.1101/2024.04.10.588904.
5
Aphid Resistance Segregates Independently of Cardenolide and Glucosinolate Content in an (Wormseed Wallflower) F2 Population.在(香芥)F2群体中,蚜虫抗性与强心甾内酯和硫代葡萄糖苷含量独立分离。
Plants (Basel). 2024 Feb 6;13(4):466. doi: 10.3390/plants13040466.
6
Cardiac glycosides protect wormseed wallflower (Erysimum cheiranthoides) against some, but not all, glucosinolate-adapted herbivores.强心苷保护野芥(Erysimum cheiranthoides)免受一些,但不是所有,含硫葡萄糖苷适应的食草动物的侵害。
New Phytol. 2024 Jun;242(6):2719-2733. doi: 10.1111/nph.19534. Epub 2024 Jan 17.
7
Cardiac glycosides protect wormseed wallflower () against some, but not all, glucosinolate-adapted herbivores.强心苷能保护香雪球免受部分(而非全部)适应硫代葡萄糖苷的食草动物的侵害。
bioRxiv. 2023 Nov 21:2023.09.19.558517. doi: 10.1101/2023.09.19.558517.
8
Toxicity of Milkweed Leaves and Latex: Chromatographic Quantification Versus Biological Activity of Cardenolides in 16 Asclepias Species.马利筋叶片和乳汁的毒性:16种马利筋属植物中强心甾类化合物的色谱定量分析与生物活性
J Chem Ecol. 2019 Jan;45(1):50-60. doi: 10.1007/s10886-018-1040-3. Epub 2018 Dec 7.
9
Cardenolides, induced responses, and interactions between above- and belowground herbivores of milkweed (Asclepias spp.).强心甾、诱导反应以及马利筋(马利筋属植物)地上与地下食草动物之间的相互作用。
Ecology. 2009 Sep;90(9):2393-404. doi: 10.1890/08-1895.1.
10
Aphid resistance segregates independently of cardiac glycoside and glucosinolate content in an (wormseed wallflower) F2 population.在一个(藜叶墙生花)F2群体中,蚜虫抗性与强心苷和硫代葡萄糖苷含量独立分离。
bioRxiv. 2024 Jan 15:2024.01.11.575310. doi: 10.1101/2024.01.11.575310.

引用本文的文献

1
A new spin on chemotaxonomy: Using non-proteogenic amino acids as a test case.化学分类学的新视角:以非蛋白质氨基酸作为一个测试案例
Appl Plant Sci. 2025 Apr 14;13(4):e70006. doi: 10.1002/aps3.70006. eCollection 2025 Jul-Aug.
2
Ipecac alkaloid biosynthesis in two evolutionarily distant plants.两种进化关系较远的植物中吐根生物碱的生物合成。
Nat Chem Biol. 2025 Jun 3. doi: 10.1038/s41589-025-01926-z.
3
Identification of UDP-dependent glycosyltransferases in the wallflower cardenolide biosynthesis pathway.在桂竹香强心苷生物合成途径中UDP依赖性糖基转移酶的鉴定。

本文引用的文献

1
New Methods to Calculate Concordance Factors for Phylogenomic Datasets.计算系统基因组数据集一致性因子的新方法。
Mol Biol Evol. 2020 Sep 1;37(9):2727-2733. doi: 10.1093/molbev/msaa106.
2
Genome sequence of the corn leaf aphid (Rhopalosiphum maidis Fitch).玉米蚜(Rhopalosiphum maidis Fitch)基因组序列。
Gigascience. 2019 Apr 1;8(4). doi: 10.1093/gigascience/giz033.
3
Toxicity of Milkweed Leaves and Latex: Chromatographic Quantification Versus Biological Activity of Cardenolides in 16 Asclepias Species.马利筋叶片和乳汁的毒性:16种马利筋属植物中强心甾类化合物的色谱定量分析与生物活性
J Biol Chem. 2025 Apr 30;301(6):108565. doi: 10.1016/j.jbc.2025.108565.
4
Plant chemical diversity enhances defense against herbivory.植物化学多样性增强了对食草动物的防御能力。
Proc Natl Acad Sci U S A. 2024 Dec 17;121(51):e2417524121. doi: 10.1073/pnas.2417524121. Epub 2024 Dec 11.
5
Four enzymes control natural variation in the steroid core of cardenolides.四种酶控制着强心苷甾体核心结构的自然变异。
bioRxiv. 2024 Apr 11:2024.04.10.588904. doi: 10.1101/2024.04.10.588904.
6
The Madagascar palm genome provides new insights on the evolution of Apocynaceae specialized metabolism.马达加斯加棕榈的基因组为夹竹桃科植物特殊代谢的进化提供了新的见解。
Heliyon. 2024 Mar 14;10(6):e28078. doi: 10.1016/j.heliyon.2024.e28078. eCollection 2024 Mar 30.
7
Aphid Resistance Segregates Independently of Cardenolide and Glucosinolate Content in an (Wormseed Wallflower) F2 Population.在(香芥)F2群体中,蚜虫抗性与强心甾内酯和硫代葡萄糖苷含量独立分离。
Plants (Basel). 2024 Feb 6;13(4):466. doi: 10.3390/plants13040466.
8
Genomes of Meniocus linifolius and Tetracme quadricornis reveal the ancestral karyotype and genomic features of core Brassicaceae.披针叶山梅花和四棱山梅花基因组揭示了核心十字花科的祖先染色体组型和基因组特征。
Plant Commun. 2024 Jul 8;5(7):100878. doi: 10.1016/j.xplc.2024.100878. Epub 2024 Mar 11.
9
Aphid resistance segregates independently of cardiac glycoside and glucosinolate content in an (wormseed wallflower) F2 population.在一个(藜叶墙生花)F2群体中,蚜虫抗性与强心苷和硫代葡萄糖苷含量独立分离。
bioRxiv. 2024 Jan 15:2024.01.11.575310. doi: 10.1101/2024.01.11.575310.
10
Cardiac glycosides protect wormseed wallflower (Erysimum cheiranthoides) against some, but not all, glucosinolate-adapted herbivores.强心苷保护野芥(Erysimum cheiranthoides)免受一些,但不是所有,含硫葡萄糖苷适应的食草动物的侵害。
New Phytol. 2024 Jun;242(6):2719-2733. doi: 10.1111/nph.19534. Epub 2024 Jan 17.
J Chem Ecol. 2019 Jan;45(1):50-60. doi: 10.1007/s10886-018-1040-3. Epub 2018 Dec 7.
4
Efficient and accurate detection of splice junctions from RNA-seq with Portcullis.使用 Portcullis 从 RNA-seq 中高效准确地检测剪接接头。
Gigascience. 2018 Dec 1;7(12):giy131. doi: 10.1093/gigascience/giy131.
5
Relative Selectivity of Plant Cardenolides for Na/K-ATPases From the Monarch Butterfly and Non-resistant Insects.植物强心甾对帝王蝶和非抗性昆虫钠钾-ATP酶的相对选择性
Front Plant Sci. 2018 Sep 28;9:1424. doi: 10.3389/fpls.2018.01424. eCollection 2018.
6
Leveraging multiple transcriptome assembly methods for improved gene structure annotation.利用多种转录组组装方法提高基因结构注释。
Gigascience. 2018 Aug 1;7(8):giy093. doi: 10.1093/gigascience/giy093.
7
ape 5.0: an environment for modern phylogenetics and evolutionary analyses in R.ape 5.0:R 中的现代系统发育学和进化分析环境。
Bioinformatics. 2019 Feb 1;35(3):526-528. doi: 10.1093/bioinformatics/bty633.
8
A multispecies coalescent model for quantitative traits.一个用于数量性状的多物种合并模型。
Elife. 2018 Aug 14;7:e36482. doi: 10.7554/eLife.36482.
9
Dissecting the basis of novel trait evolution in a radiation with widespread phylogenetic discordance.剖析在具有广泛系统发育不一致性的辐射演化中新型性状进化的基础。
Mol Ecol. 2018 Jun 28. doi: 10.1111/mec.14780.
10
Origin and maintenance of chemical diversity in a species-rich tropical tree lineage.物种丰富的热带树种系中化学多样性的起源和维持。
Nat Ecol Evol. 2018 Jun;2(6):983-990. doi: 10.1038/s41559-018-0552-0. Epub 2018 May 14.