Zhonglai Luo, Spencer C. H. Barrett, Tieyao Tu, Zhongtao Zhao, Shanshan Jia, Shiran Gu, Tingting Duan, Yu Zhang, Bingqiang Xu, Lei Gu, Xiaofang Deng, Libo Jiang, Miaomiao Shi, Dianxiang Zhang
{"title":"一个四倍体二花种中S - locus超基因的遗传结构","authors":"Zhonglai Luo, Spencer C. H. Barrett, Tieyao Tu, Zhongtao Zhao, Shanshan Jia, Shiran Gu, Tingting Duan, Yu Zhang, Bingqiang Xu, Lei Gu, Xiaofang Deng, Libo Jiang, Miaomiao Shi, Dianxiang Zhang","doi":"10.1111/nph.70521","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Heterostyly is a polymorphic floral adaptation controlled by supergenes. The molecular basis of distyly has been investigated in diploid species from several unrelated families, but information is lacking for polyploid systems.</jats:list-item> <jats:list-item>Here, we address this knowledge gap in <jats:italic>Schizomussaenda henryi</jats:italic>, a tetraploid distylous species of Rubiaceae, the family with the greatest number of heterostylous species. Using chromosome‐level genome assemblies and transcriptome profiling, we characterized its tetraploid genome, identified the <jats:italic>S</jats:italic>‐locus region, and performed evolutionary analysis.</jats:list-item> <jats:list-item>The <jats:italic>S</jats:italic>‐locus contains four hemizygous genes in the S‐morph. <jats:italic>SchzAUX22</jats:italic> emerged as a candidate gene potentially regulating both style length and filament growth via auxin signaling. Phylogenetic and <jats:italic>k</jats:italic>‐mer‐based analysis suggested a hybrid allopolyploid origin for <jats:italic>S. henryi</jats:italic>, while no subgenome dominance was detected. Results from the comparison of <jats:italic>K</jats:italic><jats:sub><jats:italic>s</jats:italic></jats:sub> values indicated that <jats:italic>S</jats:italic>‐locus formation likely occurred through stepwise duplications.</jats:list-item> <jats:list-item>This study provides the first comprehensive genomic analysis of distyly in a polyploid species and demonstrates that the <jats:italic>S</jats:italic>‐locus remains intact despite allopolyploidization resulting from hybridization. Our results indicated that polyploidization does not necessitate the breakdown of distyly, which occurs in several other heterostylous lineages.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"53 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetic architecture of the S‐locus supergene revealed in a tetraploid distylous species\",\"authors\":\"Zhonglai Luo, Spencer C. H. Barrett, Tieyao Tu, Zhongtao Zhao, Shanshan Jia, Shiran Gu, Tingting Duan, Yu Zhang, Bingqiang Xu, Lei Gu, Xiaofang Deng, Libo Jiang, Miaomiao Shi, Dianxiang Zhang\",\"doi\":\"10.1111/nph.70521\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Summary<jats:list list-type=\\\"bullet\\\"> <jats:list-item>Heterostyly is a polymorphic floral adaptation controlled by supergenes. The molecular basis of distyly has been investigated in diploid species from several unrelated families, but information is lacking for polyploid systems.</jats:list-item> <jats:list-item>Here, we address this knowledge gap in <jats:italic>Schizomussaenda henryi</jats:italic>, a tetraploid distylous species of Rubiaceae, the family with the greatest number of heterostylous species. Using chromosome‐level genome assemblies and transcriptome profiling, we characterized its tetraploid genome, identified the <jats:italic>S</jats:italic>‐locus region, and performed evolutionary analysis.</jats:list-item> <jats:list-item>The <jats:italic>S</jats:italic>‐locus contains four hemizygous genes in the S‐morph. <jats:italic>SchzAUX22</jats:italic> emerged as a candidate gene potentially regulating both style length and filament growth via auxin signaling. Phylogenetic and <jats:italic>k</jats:italic>‐mer‐based analysis suggested a hybrid allopolyploid origin for <jats:italic>S. henryi</jats:italic>, while no subgenome dominance was detected. Results from the comparison of <jats:italic>K</jats:italic><jats:sub><jats:italic>s</jats:italic></jats:sub> values indicated that <jats:italic>S</jats:italic>‐locus formation likely occurred through stepwise duplications.</jats:list-item> <jats:list-item>This study provides the first comprehensive genomic analysis of distyly in a polyploid species and demonstrates that the <jats:italic>S</jats:italic>‐locus remains intact despite allopolyploidization resulting from hybridization. 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Genetic architecture of the S‐locus supergene revealed in a tetraploid distylous species
SummaryHeterostyly is a polymorphic floral adaptation controlled by supergenes. The molecular basis of distyly has been investigated in diploid species from several unrelated families, but information is lacking for polyploid systems.Here, we address this knowledge gap in Schizomussaenda henryi, a tetraploid distylous species of Rubiaceae, the family with the greatest number of heterostylous species. Using chromosome‐level genome assemblies and transcriptome profiling, we characterized its tetraploid genome, identified the S‐locus region, and performed evolutionary analysis.The S‐locus contains four hemizygous genes in the S‐morph. SchzAUX22 emerged as a candidate gene potentially regulating both style length and filament growth via auxin signaling. Phylogenetic and k‐mer‐based analysis suggested a hybrid allopolyploid origin for S. henryi, while no subgenome dominance was detected. Results from the comparison of Ks values indicated that S‐locus formation likely occurred through stepwise duplications.This study provides the first comprehensive genomic analysis of distyly in a polyploid species and demonstrates that the S‐locus remains intact despite allopolyploidization resulting from hybridization. Our results indicated that polyploidization does not necessitate the breakdown of distyly, which occurs in several other heterostylous lineages.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.