Min Li, Jing-Jing Wu, Ren-Ping Su, Ou-Yan Fang, Xiang Cai, Pei-Han Huang, Xiao-Yang Gao, Xin-Xing Fu, Xiao-Hui Ma, Lin-Yue He, Yi-Gang Song, Guo-Xiong Hu, Shi-Shun Zhou, Yun-Hong Tan, Yves Van de Peer, Jie Li, Sheng-Dan Wu, Hong-Hu Meng
{"title":"基因组分析为恩格尔哈迪亚对东亚夏季季风的适应提供了洞见。","authors":"Min Li, Jing-Jing Wu, Ren-Ping Su, Ou-Yan Fang, Xiang Cai, Pei-Han Huang, Xiao-Yang Gao, Xin-Xing Fu, Xiao-Hui Ma, Lin-Yue He, Yi-Gang Song, Guo-Xiong Hu, Shi-Shun Zhou, Yun-Hong Tan, Yves Van de Peer, Jie Li, Sheng-Dan Wu, Hong-Hu Meng","doi":"10.1016/j.pld.2025.07.003","DOIUrl":null,"url":null,"abstract":"<p><p>Genetic information has been instrumental in elucidating the relationship between the East Asian Summer Monsoon (EASM) and subtropical evergreen broad-leaved forests (EBLFs). However, how the genomic insights of EBLFs' species correspond to environmental shifts induced by the EASM remains limited. In this study, we investigated the adaptive mechanisms of evergreen <i>Engelhardia</i> species in response to the EASM through genome sequencing and comparative genomic analyses from the <i>de novo</i> genome assemblies of five closely related <i>Engelhardia</i> taxa and one <i>Rhoiptelea</i> species. Our findings revealed that the divergence of evergreen trees from their sister deciduous species is closely associated with the onset and intensification of the EASM. This genomic transition may have coincided with a significant expansion of the terpene synthase (TPS) gene family in <i>E. fenzelii</i>, driven by four distinct modes of gene duplication. This expansion enhances the biosynthesis of terpene volatiles, providing a defensive mechanism against potential herbivory in EASM affected environments. We also identified a shared whole-genome duplication (WGD) event across <i>Engelhardia</i>, along with substantial differences in transposable element (TE) composition and activity, which contributed to genome size variation between <i>E. fenzelii</i> and <i>E. roxburghiana</i>. In addition, demographic analyses revealed a continuous population decline over the past 10 million years, further exacerbated by recent human disturbance, underscoring the conservation urgency for these species. These results not only provide preliminary insights into the complex evolutionary dynamics within the <i>Engelhardia</i> genus from genomic insights (e.g., the intricate relationships between genomic variations, environmental changes, and adaptive responses driven by significant climatic events such as the EASM), but also provides valuable insights into the conservation significance of EBLFs.</p>","PeriodicalId":20224,"journal":{"name":"Plant Diversity","volume":"47 5","pages":"718-732"},"PeriodicalIF":6.3000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12496538/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genome analyses provide insights into <i>Engelhardia</i>'s adaptation to East Asia summer monsoon.\",\"authors\":\"Min Li, Jing-Jing Wu, Ren-Ping Su, Ou-Yan Fang, Xiang Cai, Pei-Han Huang, Xiao-Yang Gao, Xin-Xing Fu, Xiao-Hui Ma, Lin-Yue He, Yi-Gang Song, Guo-Xiong Hu, Shi-Shun Zhou, Yun-Hong Tan, Yves Van de Peer, Jie Li, Sheng-Dan Wu, Hong-Hu Meng\",\"doi\":\"10.1016/j.pld.2025.07.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Genetic information has been instrumental in elucidating the relationship between the East Asian Summer Monsoon (EASM) and subtropical evergreen broad-leaved forests (EBLFs). 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Genome analyses provide insights into Engelhardia's adaptation to East Asia summer monsoon.
Genetic information has been instrumental in elucidating the relationship between the East Asian Summer Monsoon (EASM) and subtropical evergreen broad-leaved forests (EBLFs). However, how the genomic insights of EBLFs' species correspond to environmental shifts induced by the EASM remains limited. In this study, we investigated the adaptive mechanisms of evergreen Engelhardia species in response to the EASM through genome sequencing and comparative genomic analyses from the de novo genome assemblies of five closely related Engelhardia taxa and one Rhoiptelea species. Our findings revealed that the divergence of evergreen trees from their sister deciduous species is closely associated with the onset and intensification of the EASM. This genomic transition may have coincided with a significant expansion of the terpene synthase (TPS) gene family in E. fenzelii, driven by four distinct modes of gene duplication. This expansion enhances the biosynthesis of terpene volatiles, providing a defensive mechanism against potential herbivory in EASM affected environments. We also identified a shared whole-genome duplication (WGD) event across Engelhardia, along with substantial differences in transposable element (TE) composition and activity, which contributed to genome size variation between E. fenzelii and E. roxburghiana. In addition, demographic analyses revealed a continuous population decline over the past 10 million years, further exacerbated by recent human disturbance, underscoring the conservation urgency for these species. These results not only provide preliminary insights into the complex evolutionary dynamics within the Engelhardia genus from genomic insights (e.g., the intricate relationships between genomic variations, environmental changes, and adaptive responses driven by significant climatic events such as the EASM), but also provides valuable insights into the conservation significance of EBLFs.
Plant DiversityAgricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
8.30
自引率
6.20%
发文量
1863
审稿时长
35 days
期刊介绍:
Plant Diversity (formerly Plant Diversity and Resources) is an international plant science journal that publishes substantial original research and review papers that
advance our understanding of the past and current distribution of plants,
contribute to the development of more phylogenetically accurate taxonomic classifications,
present new findings on or insights into evolutionary processes and mechanisms that are of interest to the community of plant systematic and evolutionary biologists.
While the focus of the journal is on biodiversity, ecology and evolution of East Asian flora, it is not limited to these topics. Applied evolutionary issues, such as climate change and conservation biology, are welcome, especially if they address conceptual problems. Theoretical papers are equally welcome. Preference is given to concise, clearly written papers focusing on precisely framed questions or hypotheses. Papers that are purely descriptive have a low chance of acceptance.
Fields covered by the journal include:
plant systematics and taxonomy-
evolutionary developmental biology-
reproductive biology-
phylo- and biogeography-
evolutionary ecology-
population biology-
conservation biology-
palaeobotany-
molecular evolution-
comparative and evolutionary genomics-
physiology-
biochemistry