{"title":"濒危红树林物种 Acanthus ebracteatus 与 Acanthus 亲缘种之间的比较塑性体分析为其起源和适应性进化提供了启示。","authors":"Zanshan Fang, Danfeng Li, Haien Murong, Meng He, Yuqi Liu, Jiaxuan Liu, Jiaxiao Wu, Yingqi Li, Yongyu Li, Xiang Jin, Yuchen Yang, Ying Zhang","doi":"10.1002/ece3.70566","DOIUrl":null,"url":null,"abstract":"<p><i>Acanthus ebracteatus</i> is a typical true mangrove species with great ecological and medicinal values. However, it has become endangered in China. Moreover, because of the similar morphology and distribution, it is commonly confused with the congeneric mangrove species, <i>A. ilicifolius</i>, which poses challenges to the protection and proper medicinal utilization of <i>A. ebracteatus</i>. Plastomes provide a solution for molecular identification and adaptive evolution investigation of plants. In this study, we dissected the complete plastome for <i>A. ebracteatus</i> and performed comparative analysis to <i>A. ilicifolius</i> and three non-mangrove relatives (<i>A. montanus</i>, <i>A. leucostachyus</i> and <i>A. mollis</i>). Both plastome sequences and structure are highly conserved between the two mangrove species, while less similar between mangrove and non-mangrove species. Phylogenetic analysis suggested that the mangrove species were divergent from the non-mangrove groups at approximately 15.15 million years ago (Mya), where early to middle Miocene global warming and high sea level might act as one of the main forces driving the mangrove lineage entering into intertidal environments. Furthermore, 12 single nucleotide polymorphisms (SNPs) and 10 insertions/deletions (indels) were detected between the plastomes of <i>A. ebracteatus</i> and <i>A. ilicifolius</i>. PCR validation further demonstrated the effectiveness of the plastid marker in distinguishing the two sibling mangrove species. Taken together, our study broadens the understanding of the origin and evolution of <i>Acanthus</i> mangrove plants, and provided valuable information on the correct identification and protection of endangered mangrove species <i>A. ebracteatus</i>.</p>","PeriodicalId":11467,"journal":{"name":"Ecology and Evolution","volume":"14 11","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578654/pdf/","citationCount":"0","resultStr":"{\"title\":\"Comparative Plastome Analysis Between Endangered Mangrove Species Acanthus ebracteatus and Acanthus Relatives Provides Insights into Its Origin and Adaptive Evolution\",\"authors\":\"Zanshan Fang, Danfeng Li, Haien Murong, Meng He, Yuqi Liu, Jiaxuan Liu, Jiaxiao Wu, Yingqi Li, Yongyu Li, Xiang Jin, Yuchen Yang, Ying Zhang\",\"doi\":\"10.1002/ece3.70566\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Acanthus ebracteatus</i> is a typical true mangrove species with great ecological and medicinal values. However, it has become endangered in China. Moreover, because of the similar morphology and distribution, it is commonly confused with the congeneric mangrove species, <i>A. ilicifolius</i>, which poses challenges to the protection and proper medicinal utilization of <i>A. ebracteatus</i>. Plastomes provide a solution for molecular identification and adaptive evolution investigation of plants. In this study, we dissected the complete plastome for <i>A. ebracteatus</i> and performed comparative analysis to <i>A. ilicifolius</i> and three non-mangrove relatives (<i>A. montanus</i>, <i>A. leucostachyus</i> and <i>A. mollis</i>). Both plastome sequences and structure are highly conserved between the two mangrove species, while less similar between mangrove and non-mangrove species. Phylogenetic analysis suggested that the mangrove species were divergent from the non-mangrove groups at approximately 15.15 million years ago (Mya), where early to middle Miocene global warming and high sea level might act as one of the main forces driving the mangrove lineage entering into intertidal environments. Furthermore, 12 single nucleotide polymorphisms (SNPs) and 10 insertions/deletions (indels) were detected between the plastomes of <i>A. ebracteatus</i> and <i>A. ilicifolius</i>. PCR validation further demonstrated the effectiveness of the plastid marker in distinguishing the two sibling mangrove species. Taken together, our study broadens the understanding of the origin and evolution of <i>Acanthus</i> mangrove plants, and provided valuable information on the correct identification and protection of endangered mangrove species <i>A. ebracteatus</i>.</p>\",\"PeriodicalId\":11467,\"journal\":{\"name\":\"Ecology and Evolution\",\"volume\":\"14 11\",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578654/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ecology and Evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ece3.70566\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece3.70566","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
白刺芒(Acanthus ebracteatus)是一种典型的真红树物种,具有极高的生态和药用价值。然而,它在中国已濒临灭绝。此外,由于形态和分布相似,它通常会与同属的红树林物种 A. ilicifolius 混淆,这给白花蛇舌草的保护和合理药用带来了挑战。植物体为植物的分子鉴定和适应性进化研究提供了解决方案。在这项研究中,我们剖析了白术的完整质体,并与白术和三种非红树亲缘植物(A. montanus、A. leucostachyus 和 A. mollis)进行了比较分析。两个红树林物种之间的质体序列和结构都高度保守,而红树林和非红树林物种之间的相似性较低。系统发育分析表明,红树林物种大约在 1515 万年前与非红树林类群分化,中新世早中期的全球变暖和高海平面可能是促使红树林物种进入潮间带环境的主要原因之一。此外,研究人员还检测了A. ebracteatus和A. ilicifolius质粒之间的12个单核苷酸多态性(SNPs)和10个插入/缺失(indels)。PCR 验证进一步证明了质体标记在区分两个同胞红树林物种方面的有效性。总之,我们的研究拓宽了对红树Acanthus起源和进化的认识,为正确识别和保护濒危红树物种A. ebracteatus提供了宝贵信息。
Comparative Plastome Analysis Between Endangered Mangrove Species Acanthus ebracteatus and Acanthus Relatives Provides Insights into Its Origin and Adaptive Evolution
Acanthus ebracteatus is a typical true mangrove species with great ecological and medicinal values. However, it has become endangered in China. Moreover, because of the similar morphology and distribution, it is commonly confused with the congeneric mangrove species, A. ilicifolius, which poses challenges to the protection and proper medicinal utilization of A. ebracteatus. Plastomes provide a solution for molecular identification and adaptive evolution investigation of plants. In this study, we dissected the complete plastome for A. ebracteatus and performed comparative analysis to A. ilicifolius and three non-mangrove relatives (A. montanus, A. leucostachyus and A. mollis). Both plastome sequences and structure are highly conserved between the two mangrove species, while less similar between mangrove and non-mangrove species. Phylogenetic analysis suggested that the mangrove species were divergent from the non-mangrove groups at approximately 15.15 million years ago (Mya), where early to middle Miocene global warming and high sea level might act as one of the main forces driving the mangrove lineage entering into intertidal environments. Furthermore, 12 single nucleotide polymorphisms (SNPs) and 10 insertions/deletions (indels) were detected between the plastomes of A. ebracteatus and A. ilicifolius. PCR validation further demonstrated the effectiveness of the plastid marker in distinguishing the two sibling mangrove species. Taken together, our study broadens the understanding of the origin and evolution of Acanthus mangrove plants, and provided valuable information on the correct identification and protection of endangered mangrove species A. ebracteatus.
期刊介绍:
Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment.
Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.