Anthony Côrtes Gomes, Jacob Montgomery, André Lucas Simões Araujo, Sarah Morran, Luan Cutti, Eric Patterson, Sofia Marques Hill, Maor Matzrafi, Anil Shrestha, Aldo Merotto, Fatemeh Abdollahi, David R Nelson, Victor Llaca, Kevin Fengler, Camila Ferreira de Pinho, Todd A Gaines
{"title":"Chromosome-level assemblies of the allohexaploid genomes of Conyza sumatrensis and Conyza bonariensis.","authors":"Anthony Côrtes Gomes, Jacob Montgomery, André Lucas Simões Araujo, Sarah Morran, Luan Cutti, Eric Patterson, Sofia Marques Hill, Maor Matzrafi, Anil Shrestha, Aldo Merotto, Fatemeh Abdollahi, David R Nelson, Victor Llaca, Kevin Fengler, Camila Ferreira de Pinho, Todd A Gaines","doi":"10.1093/gbe/evaf065","DOIUrl":null,"url":null,"abstract":"<p><p>Conyza sumatrensis and Conyza bonariensis are two important hexaploid weed species that impact crop production systems across the globe. Here, we report reference genome assemblies for both species. The sequenced accession of C. sumatrensis is resistant to multiple herbicides and was collected from the state of Paraná in Brazil, while the accession of C. bonariensis was collected from California, USA. Genomic long read data was used along with optical mapping data to assemble the C. sumatrensis genome to a single haplome at chromosome-level contiguity. The same approach was used along with chromatin contact mapping data to phase the haplotypes of C. bonariensis and generate two chromosome-level haplome assemblies. Subgenome specific sequences were identified and used to classify the three subgenomes within each assembly. The assemblies are highly complete based on the presence of conserved single copy orthologs and telomeres, and the size of these assemblies agree with previous flow cytometry estimates. Full length transcript sequencing along with gene models from other Asteraceae members were used to predict gene models within each assembly. The genomic resources reported here will be useful for investigations into evolutionary and ecological questions around weed invasion and management for these two species.</p>","PeriodicalId":12779,"journal":{"name":"Genome Biology and Evolution","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome Biology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/gbe/evaf065","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Conyza sumatrensis and Conyza bonariensis are two important hexaploid weed species that impact crop production systems across the globe. Here, we report reference genome assemblies for both species. The sequenced accession of C. sumatrensis is resistant to multiple herbicides and was collected from the state of Paraná in Brazil, while the accession of C. bonariensis was collected from California, USA. Genomic long read data was used along with optical mapping data to assemble the C. sumatrensis genome to a single haplome at chromosome-level contiguity. The same approach was used along with chromatin contact mapping data to phase the haplotypes of C. bonariensis and generate two chromosome-level haplome assemblies. Subgenome specific sequences were identified and used to classify the three subgenomes within each assembly. The assemblies are highly complete based on the presence of conserved single copy orthologs and telomeres, and the size of these assemblies agree with previous flow cytometry estimates. Full length transcript sequencing along with gene models from other Asteraceae members were used to predict gene models within each assembly. The genomic resources reported here will be useful for investigations into evolutionary and ecological questions around weed invasion and management for these two species.
期刊介绍:
About the journal
Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.