Hongbing Liu, Hang Zhao, Yanwen Zhang, Xiuli Li, Yi Zuo, Zhen Wu, Kaining Jin, Wenfei Xian, Wenzheng Wang, Weidong Ning, Zijian Liu, Xiaoxiao Zhao, Lei Wang, Rowan F. Sage, Tiegang Lu, Matt Stata, Shifeng Cheng
{"title":"Eleocharis vivipara 的基因组阐明了 C3-C4 光合可塑性的遗传学以及香柏科植物核型的进化。","authors":"Hongbing Liu, Hang Zhao, Yanwen Zhang, Xiuli Li, Yi Zuo, Zhen Wu, Kaining Jin, Wenfei Xian, Wenzheng Wang, Weidong Ning, Zijian Liu, Xiaoxiao Zhao, Lei Wang, Rowan F. Sage, Tiegang Lu, Matt Stata, Shifeng Cheng","doi":"10.1111/jipb.13765","DOIUrl":null,"url":null,"abstract":"<p><i>Eleocharis vivipara</i>, an amphibious sedge in the Cyperaceae family, has several remarkable properties, most notably its alternate use of C<sub>3</sub> photosynthesis underwater and C<sub>4</sub> photosynthesis on land. However, the absence of genomic data has hindered its utility for evolutionary and genetic research. Here, we present a high-quality genome for <i>E. vivipara</i>, representing the first chromosome-level genome for the <i>Eleocharis</i> genus, with an approximate size of 965.22 Mb mainly distributed across 10 chromosomes. Its Hi–C pattern, chromosome clustering results, and one-to-one genome synteny across two subgroups indicates a tetraploid structure with chromosome count 2<i>n</i> = 4<i>x</i> = 20. Phylogenetic analysis suggests that <i>E. vivipara</i> diverged from <i>Cyperus esculentus</i> approximately 32.96 million years ago (Mya), and underwent a whole-genome duplication (WGD) about 3.5 Mya. Numerous fusion and fission events were identified between the chromosomes of <i>E. vivipara</i> and its close relatives. We demonstrate that <i>E. vivipara</i> has holocentromeres, a chromosomal feature which can maintain the stability of such chromosomal rearrangements. Experimental transplantation and cross-section studies showed its terrestrial culms developed C<sub>4</sub> Kranz anatomy with increased number of chloroplasts in the bundle sheath (BS) cells. Gene expression and weighted gene co-expression network analysis (WGCNA) showed overall elevated expression of core genes associated with the C<sub>4</sub> pathway, and significant enrichment of genes related to modified culm anatomy and photosynthesis efficiency. We found evidence of mixed nicotinamide adenine dinucleotide - malic enzyme and phosphoenolpyruvate carboxykinase type C<sub>4</sub> photosynthesis in <i>E. vivipara</i>, and hypothesize that the evolution of C<sub>4</sub> photosynthesis predates the WGD event. The mixed type is dominated by subgenome A and supplemented by subgenome B. Collectively, our findings not only shed light on the evolution of <i>E. vivipara</i> and karyotype within the Cyperaceae family, but also provide valuable insights into the transition between C<sub>3</sub> and C<sub>4</sub> photosynthesis, offering promising avenues for crop improvement and breeding.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":"66 11","pages":"2505-2527"},"PeriodicalIF":9.3000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jipb.13765","citationCount":"0","resultStr":"{\"title\":\"The genome of Eleocharis vivipara elucidates the genetics of C3–C4 photosynthetic plasticity and karyotype evolution in the Cyperaceae\",\"authors\":\"Hongbing Liu, Hang Zhao, Yanwen Zhang, Xiuli Li, Yi Zuo, Zhen Wu, Kaining Jin, Wenfei Xian, Wenzheng Wang, Weidong Ning, Zijian Liu, Xiaoxiao Zhao, Lei Wang, Rowan F. Sage, Tiegang Lu, Matt Stata, Shifeng Cheng\",\"doi\":\"10.1111/jipb.13765\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Eleocharis vivipara</i>, an amphibious sedge in the Cyperaceae family, has several remarkable properties, most notably its alternate use of C<sub>3</sub> photosynthesis underwater and C<sub>4</sub> photosynthesis on land. However, the absence of genomic data has hindered its utility for evolutionary and genetic research. Here, we present a high-quality genome for <i>E. vivipara</i>, representing the first chromosome-level genome for the <i>Eleocharis</i> genus, with an approximate size of 965.22 Mb mainly distributed across 10 chromosomes. Its Hi–C pattern, chromosome clustering results, and one-to-one genome synteny across two subgroups indicates a tetraploid structure with chromosome count 2<i>n</i> = 4<i>x</i> = 20. Phylogenetic analysis suggests that <i>E. vivipara</i> diverged from <i>Cyperus esculentus</i> approximately 32.96 million years ago (Mya), and underwent a whole-genome duplication (WGD) about 3.5 Mya. Numerous fusion and fission events were identified between the chromosomes of <i>E. vivipara</i> and its close relatives. We demonstrate that <i>E. vivipara</i> has holocentromeres, a chromosomal feature which can maintain the stability of such chromosomal rearrangements. Experimental transplantation and cross-section studies showed its terrestrial culms developed C<sub>4</sub> Kranz anatomy with increased number of chloroplasts in the bundle sheath (BS) cells. Gene expression and weighted gene co-expression network analysis (WGCNA) showed overall elevated expression of core genes associated with the C<sub>4</sub> pathway, and significant enrichment of genes related to modified culm anatomy and photosynthesis efficiency. We found evidence of mixed nicotinamide adenine dinucleotide - malic enzyme and phosphoenolpyruvate carboxykinase type C<sub>4</sub> photosynthesis in <i>E. vivipara</i>, and hypothesize that the evolution of C<sub>4</sub> photosynthesis predates the WGD event. The mixed type is dominated by subgenome A and supplemented by subgenome B. 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The genome of Eleocharis vivipara elucidates the genetics of C3–C4 photosynthetic plasticity and karyotype evolution in the Cyperaceae
Eleocharis vivipara, an amphibious sedge in the Cyperaceae family, has several remarkable properties, most notably its alternate use of C3 photosynthesis underwater and C4 photosynthesis on land. However, the absence of genomic data has hindered its utility for evolutionary and genetic research. Here, we present a high-quality genome for E. vivipara, representing the first chromosome-level genome for the Eleocharis genus, with an approximate size of 965.22 Mb mainly distributed across 10 chromosomes. Its Hi–C pattern, chromosome clustering results, and one-to-one genome synteny across two subgroups indicates a tetraploid structure with chromosome count 2n = 4x = 20. Phylogenetic analysis suggests that E. vivipara diverged from Cyperus esculentus approximately 32.96 million years ago (Mya), and underwent a whole-genome duplication (WGD) about 3.5 Mya. Numerous fusion and fission events were identified between the chromosomes of E. vivipara and its close relatives. We demonstrate that E. vivipara has holocentromeres, a chromosomal feature which can maintain the stability of such chromosomal rearrangements. Experimental transplantation and cross-section studies showed its terrestrial culms developed C4 Kranz anatomy with increased number of chloroplasts in the bundle sheath (BS) cells. Gene expression and weighted gene co-expression network analysis (WGCNA) showed overall elevated expression of core genes associated with the C4 pathway, and significant enrichment of genes related to modified culm anatomy and photosynthesis efficiency. We found evidence of mixed nicotinamide adenine dinucleotide - malic enzyme and phosphoenolpyruvate carboxykinase type C4 photosynthesis in E. vivipara, and hypothesize that the evolution of C4 photosynthesis predates the WGD event. The mixed type is dominated by subgenome A and supplemented by subgenome B. Collectively, our findings not only shed light on the evolution of E. vivipara and karyotype within the Cyperaceae family, but also provide valuable insights into the transition between C3 and C4 photosynthesis, offering promising avenues for crop improvement and breeding.
期刊介绍:
Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.