Abstract
The cultivation and domestication of roses reflects cultural exchanges and shifts in aesthetics that have resulted in today’s most popular ornamental plant group. However, the narrow genetic foundation of cultivated roses limits their further improvement. Wild Rosa species harbour vast genetic diversity, yet their utilization is impeded by taxonomic confusion. Here we generated a phased and gap-free reference genome of Rosa persica for phylogenetic and population genomic analyses of a large collection of Rosa samples. The robust nuclear and plastid phylogenies support most of the morphology-based traditional taxonomy of Rosa. Population genomic analyses disclosed potential genetic exchanges among sections, indicating the northwest and southwest of China as two independent centres of diversity for Rosa. Analyses of domestication traits provide insights into selection processes related to flower colour, fragrance, double flower and resistance. This study provides a comprehensive understanding of rose domestication and lays a solid foundation for future re-domestication and innovative breeding efforts using wild resources.
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Data availability
Raw sequencing data have been deposited in the National Center for Biotechnology Information (NCBI) BioProject database with the BioProject PRJNA1224503. The phased genome assembly of R. persica has been deposited in the NCBI database under accession numbers JBLIYO000000000 (Hap 1) and JBLIYP000000000 (Hap 2). The previously published reads used in this study are available from NCBI and public GDR database at https://www.rosaceae.org. Specific source data are listed in Supplementary Tables 10 and 13.
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Acknowledgements
We thank Y. Yang (Kunming Yang Chinese Rose Gardening) for collecting wild Rosa resources and for helpful discussions on Rosa taxonomy. We are grateful to Y. Sui and R. Guo (Xinjiang Career Technical College) for their efforts in collecting Rosa resources in Xinjiang. We thank X. Gao (Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University) for his inspiring discussion and comments. We appreciate the valuable suggestions on the manuscript provided by R. Smulders and P. Arens (Plant Breeding, Wageningen University and Research). We thank J. Endelman (University of Wisconsin) for his instruction on GWASpoly software. We thank Man Zhang and T. Zheng for the suggestions on improving the paper. We thank J. Zhao (Boyce Thompson Institute) for his instruction on demographic analyses. We thank Yuxuan Zhang, L. Ji, Yujing Zhang, L. Jiang, C. Feng, Y. Zhuang, Z. Ou, R. Wang, J. Tang and K. Xiong for their assistance with the investigations of Rosa species. Furthermore, we thank Wuhan Dazhong Yuansheng Technology, Wuhan Feisha Genetic Information (www.frasergen.com) and BerryGenomics (www.berrygenomics.com) for providing essential sequencing service. Finally, the authors are profoundly indebted to every member of the Fishpond family, whose collective efforts were instrumental in the fruition of this work. This research was supported by the Fundamental Research Funds for the Central Universities (grant number QNTD202306 to C. Yu), National Key R&D Program of China (grant number 2019YFD1000400 to C. Yu) and National Natural Science Foundation of China (grant numbers 32471955 and 32071818 to C. Yu).
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C. Yu designed and managed the project. B.C. performed population genomic analyses and wrote the manuscript. K.Z. assembled the Rosa persica genome and performed genomic analyses. M.Z. performed GWAS analysis. P.M.B. provided guidance on GWAS analysis and revised the manuscript. L. Zhou and Y.S. managed the plant materials. S.W. performed population history analyses. L.G. performed selective sweep analyses. W.D. performed demographic analyses. C. Yang and J.C. constructed phylogenetic trees and performed phylogenetic analyses. R.H. designed and revised the figures. X.T. performed karyotype analyses of Rosa materials. L. Zhang performed data analyses. C. Yu, B.C., K.Z., M.Z., L.G., W.D. and S.W. wrote the paper with contributions from H.H., Y.H., L.L., H.P. and Q.Z.
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Extended data
Extended Data Fig. 1 Flower traits of Rosa accessions used in this study.
The plates of accessions are sorted by scientific groups. Sample IDs correspond to Supplementary Table 13.
Extended Data Fig. 2 Leaf traits of Rosa accessions used in this study.
The plates of accessions are sorted by number of leaflets. Sample IDs correspond to Supplementary Table 13.
Extended Data Fig. 3 Comparison between plastid phylogeny (left) based on chloroplast coding sequences, and nuclear phylogeny (right) based on single-copy SNPs.
Both trees were constructed using maximum likelihood method. Bootstrap values were tested with 1,000 replicates. The colors represent accessions from different botanical groups, in correspondence with previous figures.
Extended Data Fig. 4 Geographical distributions of different botanical sections of Rosa.
The white dots represent distribution information of Rosa accessions, which was derived from field investigation, specimen information, and geographic distribution records from Flora of China and Chinese Virtual Herbarium (http://www.cvh.ac.cn).
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Supplementary Figs. 1–12, notes and methods.
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Supplementary Tables 1–20.
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Cheng, B., Zhao, K., Zhou, M. et al. Phenotypic and genomic signatures across wild Rosa species open new horizons for modern rose breeding. Nat. Plants 11, 775–789 (2025). https://doi.org/10.1038/s41477-025-01955-5
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DOI: https://doi.org/10.1038/s41477-025-01955-5
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