The genome of Eleocharis vivipara elucidates the genetics of C-C photosynthetic plasticity and karyotype evolution in the Cyperaceae.

Lei Wang, Matt Stata, Tiegang Lu, Weidong Ning, Wenzheng Wang, Wenfei Xian, Kaining Jin, Xiuli Li, Yanwen Zhang, Yi Zuo, Zhen Wu, Hang Zhao, Hongbing Liu, Zijian Liu, Rowan F Sage, Shifeng Cheng, Xiaoxiao Zhao

Journal: Journal of integrative plant biology 2024;66(11):2505-2527

PMID: 39177373

Abstract

Eleocharis vivipara, an amphibious sedge in the Cyperaceae family, has several remarkable properties, most notably its alternate use of C photosynthesis underwater and C 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 C 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 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 photosynthesis in E. vivipara, and hypothesize that the evolution of C 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 C and C photosynthesis, offering promising avenues for crop improvement and breeding.

© 2024 The Author(s). Journal of Integrative Plant Biology published by John Wiley & Sons Australia, Ltd on behalf of Institute of Botany, Chinese Academy of Sciences.

Address: Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.; Gembloux Agro-Bio Tech, TERRA Teaching and Research Centre, University of Liège, Gembloux, 4000, Belgium.; Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.; State Key Laboratory of Crop Stress Adaptation and Improvement, School of Life Sciences, Henan University, Kaifeng, 475004, China.; Shenzhen Research Institute of Henan university, Shenzhen, 518000, China.; Key Laboratory of Plant Molecular Physiology, Institute of Botany, China National Botanical Garden, Chinese Academy of Science, Beijing, 100093, China.; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.; Department of Plant Sciences, Centre for Crop Systems Analysis, Wageningen University & Research, Wageningen, 6708 WB, The Netherlands.; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.; Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.; Gembloux Agro-Bio Tech, TERRA Teaching and Research Centre, University of Liège, Gembloux, 4000, Belgium.; Department of Ecology and Evolutionary Biology, The University of Toronto, Toronto, M5S 3B2, ON, Canada.; Plant Resilience Institute, Michigan State University, East Lansing, 48824, MI, USA.; Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, 48824, MI, USA.

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