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Generating Homo- and Heterografts Between Watermelon and Bottle Gourd for the Study of Cold-responsive MicroRNAs
Published on: November 20, 2018
Telomere-to-telomere genome assembly and comprehensive mutation library facilitate bitter gourd breeding and
Yilin Zhang1, Xiaoyi Wang2, Yan Wang3
1National Key Laboratory of Wheat Improvement, Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences at Weifang, Weifang 261000, China; Laboratory of Plant and Environment Interaction Study, Tsientang Institute for Advanced Study, Hangzhou 310024, China; State Key Laboratory of Protein and Plant Gene Research, School of Advanced Agricultural Sciences and School of Life Sciences, Peking University, Beijing 100871, China; College of Life Sciences, Zhejiang University, Hangzhou 310058, China.
Abstract:
Bitter gourd (Momordica charantia) is an economically important vegetable crop with notable medicinal properties, yet its genetic improvement has been hindered by limited genomic resources and insufficient functional genomics tools. Here, we present a comprehensive genomic and functional resource platform to address these limitations. Using PacBio HiFi and Oxford Nanopore ultra-long sequencing technologies combined with Hi-C, we generated a telomere-to-telomere (T2T), gap-free genome assembly of the elite bitter gourd cultivar Y52, comprising 11 chromosomes with a final assembly size of 298.0 Mb. This high-quality assembly enabled precise annotation of complex genomic regions, including centromeres characterized through chromatin immunoprecipitation sequencing. We further constructed a large-scale ethyl methanesulfonate (EMS)-induced mutant library consisting of 3223 M1 plants and performed whole-genome resequencing of 320 mutants, identifying approximately 76 002 induced mutations affecting 13 984 genes. Using this mutant population, we rapidly identified the causal gene McEGY1, responsible for chlorotic leaf and fruit phenotypes, through a MutMap-based approach. In addition, we conducted bulked segregant analysis and bulked segregant RNA sequencing to identify genomic regions and candidate genes associated with key agronomic traits, including fruit length, fruit tubercle formation, and powdery mildew resistance. Moreover, integrated transcriptomic and metabolomic analyses across multiple tissues and developmental stages generated comprehensive profiles of gene expression and metabolite accumulation, revealing tissue-specific regulatory networks. Finally, we integrated the genomic, mutant, transcriptomic, and metabolomic resources generated in this study to establish Bittergourd DB, a comprehensive platform supporting bitter gourd functional genomics and molecular breeding. Collectively, this study provides an unprecedented genomic and functional resource for bitter gourd, including a complete T2T reference genome, an extensive EMS mutant library, trait-associated loci, and multi-omics maps, which will substantially accelerate functional genomics research and molecular breeding in this species.
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