Yair Cárdenas-Conejo, Gerardo Rafael Argüello-Astorga, Daniel Alejandro García-Rodríguez, Daniel Alejandro Mendoza-Magaña, Bernardo Bañuelos-Hernández, Sara Centeno-Leija, Hugo Serrano-Posada, Laura Angélica Espinosa-Barrera, Edith Elena Uresti-Rivera, Raúl Loera-Valencia
{"title":"杜鹃花属的内源性双病毒样元件为begomvirus核穿梭蛋白的进化起源提供了见解。","authors":"Yair Cárdenas-Conejo, Gerardo Rafael Argüello-Astorga, Daniel Alejandro García-Rodríguez, Daniel Alejandro Mendoza-Magaña, Bernardo Bañuelos-Hernández, Sara Centeno-Leija, Hugo Serrano-Posada, Laura Angélica Espinosa-Barrera, Edith Elena Uresti-Rivera, Raúl Loera-Valencia","doi":"10.1007/s11103-025-01609-2","DOIUrl":null,"url":null,"abstract":"<p><p>Geminiviruses constitute a diverse group of plant viruses with small, circular single-stranded DNA genomes. While most geminiviruses possess monopartite genomes, the genus Begomovirus uniquely includes both monopartite and bipartite members. The evolutionary origin of the second component of begomovirus (DNA-B) has been a subject of considerable debate. Two primary hypotheses propose that DNA-B originated from a modified monopartite genome or through the capture of a satellite DNA. Recent discoveries of unclassified bipartite geminiviruses call for a reevaluation of these hypotheses. To address this, we investigated the evolutionary history of the begomovirus nuclear shuttle protein (NSP) through homolog searches, comparative genomics, and structural protein analyses. Our findings unambiguously demonstrated that NSP is homologous to the coat protein (CP) but originated from a CP encoded by an ancient geminivirus lineage, distinct from begomoviruses. This ancient lineage is represented by bipartite viruses integrated into plant genomes of the genus Rhododendron. These results challenge the prevailing paradigm regarding the evolutionary origin of NSP and offer new insights into the evolution of begomovirus genome architecture.</p>","PeriodicalId":20064,"journal":{"name":"Plant Molecular Biology","volume":"115 4","pages":"81"},"PeriodicalIF":3.9000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Endogenous geminivirus-like elements in the genus Rhododendron provide insights into the evolutionary origins of the begomovirus nuclear shuttle protein.\",\"authors\":\"Yair Cárdenas-Conejo, Gerardo Rafael Argüello-Astorga, Daniel Alejandro García-Rodríguez, Daniel Alejandro Mendoza-Magaña, Bernardo Bañuelos-Hernández, Sara Centeno-Leija, Hugo Serrano-Posada, Laura Angélica Espinosa-Barrera, Edith Elena Uresti-Rivera, Raúl Loera-Valencia\",\"doi\":\"10.1007/s11103-025-01609-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Geminiviruses constitute a diverse group of plant viruses with small, circular single-stranded DNA genomes. While most geminiviruses possess monopartite genomes, the genus Begomovirus uniquely includes both monopartite and bipartite members. The evolutionary origin of the second component of begomovirus (DNA-B) has been a subject of considerable debate. Two primary hypotheses propose that DNA-B originated from a modified monopartite genome or through the capture of a satellite DNA. Recent discoveries of unclassified bipartite geminiviruses call for a reevaluation of these hypotheses. To address this, we investigated the evolutionary history of the begomovirus nuclear shuttle protein (NSP) through homolog searches, comparative genomics, and structural protein analyses. Our findings unambiguously demonstrated that NSP is homologous to the coat protein (CP) but originated from a CP encoded by an ancient geminivirus lineage, distinct from begomoviruses. This ancient lineage is represented by bipartite viruses integrated into plant genomes of the genus Rhododendron. These results challenge the prevailing paradigm regarding the evolutionary origin of NSP and offer new insights into the evolution of begomovirus genome architecture.</p>\",\"PeriodicalId\":20064,\"journal\":{\"name\":\"Plant Molecular Biology\",\"volume\":\"115 4\",\"pages\":\"81\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s11103-025-01609-2\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s11103-025-01609-2","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Endogenous geminivirus-like elements in the genus Rhododendron provide insights into the evolutionary origins of the begomovirus nuclear shuttle protein.
Geminiviruses constitute a diverse group of plant viruses with small, circular single-stranded DNA genomes. While most geminiviruses possess monopartite genomes, the genus Begomovirus uniquely includes both monopartite and bipartite members. The evolutionary origin of the second component of begomovirus (DNA-B) has been a subject of considerable debate. Two primary hypotheses propose that DNA-B originated from a modified monopartite genome or through the capture of a satellite DNA. Recent discoveries of unclassified bipartite geminiviruses call for a reevaluation of these hypotheses. To address this, we investigated the evolutionary history of the begomovirus nuclear shuttle protein (NSP) through homolog searches, comparative genomics, and structural protein analyses. Our findings unambiguously demonstrated that NSP is homologous to the coat protein (CP) but originated from a CP encoded by an ancient geminivirus lineage, distinct from begomoviruses. This ancient lineage is represented by bipartite viruses integrated into plant genomes of the genus Rhododendron. These results challenge the prevailing paradigm regarding the evolutionary origin of NSP and offer new insights into the evolution of begomovirus genome architecture.
期刊介绍:
Plant Molecular Biology is an international journal dedicated to rapid publication of original research articles in all areas of plant biology.The Editorial Board welcomes full-length manuscripts that address important biological problems of broad interest, including research in comparative genomics, functional genomics, proteomics, bioinformatics, computational biology, biochemical and regulatory networks, and biotechnology. Because space in the journal is limited, however, preference is given to publication of results that provide significant new insights into biological problems and that advance the understanding of structure, function, mechanisms, or regulation. Authors must ensure that results are of high quality and that manuscripts are written for a broad plant science audience.