Artur Teixeira de Araujo, Rashmi Jain, Deling Ruan, Mawsheng Chern, Nguyen Ho, Rohan Bhushan Jhingan, Guotian Li, Phat Q Duong, Maria Florencia Ercoli, Pamela C Ronald
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引用次数: 0
Abstract
Fast-neutron mutagenesis creates diverse genome-wide mutations, providing a powerful tool for crop functional genomics. Here, we present an expanded genomic and phenotypic analysis of 3268 fast-neutron (FN)-induced mutant rice lines (Oryza sativa L. cv. Kitaake). All FN lines were whole-genome sequenced, and mutations were identified by alignment in the Nipponbare and KitaakeX reference genomes. We cataloged over 428,000 mutations affecting 78.49% of Nipponbare genes and 70.38% of KitaakeX genes. In silico expression analysis indicates that 575 non-mutated Nipponbare genes are highly expressed and likely essential for viability. Each mutant carries, on average, 68.5 mutations in the Nipponbare alignments or 63.2 mutations for KitaakeX alignments, distributed randomly across all 12 chromosomes with no evident hotspots. FN lines have approximately 8.5% fewer mutations when using the KitaakeX alignment, underscoring the unique contributions of each reference genome and the importance of utilizing both for comprehensive mutation discovery. The majority of mutations are small deletions and single-base substitutions, with deletions predominating in their effect on genes. We found that 74.4% of all transcription factor Nipponbare genes were mutated at least once. Phenotypic characterization of over 2700 lines revealed a broad spectrum of variation in core agronomic traits (heading date, tiller number, plant height, panicle weight, seed yield components) and other morphological variants of interest. The integration of genomic and phenotypic data through the KitBase platform enabled the identification of candidate genes for several traits of interest. The KitBase website (https://kitbase.ucdavis.edu) has been updated to provide open access to all mutation data and seed stocks, as well as an intuitive query interface, facilitating forward and reverse genetic analyses in rice. This expanded resource enriches the rice functional genomics toolkit and highlights the value of coupling high-density mutation mapping with phenotypic data for rapid gene discovery and crop improvement.
快中子诱变产生了多种全基因组突变,为作物功能基因组学研究提供了有力的工具。在此,我们对3268个快中子(FN)诱导突变水稻品系(Oryza sativa L. cv.)进行了扩展的基因组和表型分析。Kitaake)。对所有FN系进行全基因组测序,并通过比对Nipponbare和KitaakeX参考基因组来鉴定突变。我们编目了超过428,000个突变,影响78.49%的Nipponbare基因和70.38%的KitaakeX基因。硅表达分析表明575个非突变的Nipponbare基因高度表达,可能是生存所必需的。每个突变体平均携带68.5个Nipponbare突变体和63.2个KitaakeX突变体,随机分布在所有12条染色体上,没有明显的热点。当使用KitaakeX序列时,FN系的突变减少了约8.5%,强调了每个参考基因组的独特贡献以及利用两者进行全面突变发现的重要性。大多数突变是小的缺失和单碱基替换,缺失在它们对基因的影响中占主导地位。我们发现74.4%的转录因子Nipponbare基因至少发生了一次突变。对2700多个品系的表型分析显示,在抽穗日期、分蘖数、株高、穗重、籽粒产量等核心农艺性状和其他感兴趣的形态变异方面存在广泛的变异。通过KitBase平台整合基因组和表型数据,可以识别出几种感兴趣的性状的候选基因。KitBase网站(https://kitbase.ucdavis.edu)已更新,提供对所有突变数据和种子库存的开放访问,以及直观的查询界面,促进水稻的正向和反向遗传分析。这一扩展的资源丰富了水稻功能基因组学工具包,并突出了高密度突变定位与表型数据耦合在快速基因发现和作物改良中的价值。
期刊介绍:
Huge volumes of primary data are archived in numerous open-access databases, and with new generation technologies becoming more common in laboratories, large datasets will become even more prevalent. The archiving, curation, analysis and interpretation of all of these data are a challenge. Database development and biocuration are at the forefront of the endeavor to make sense of this mounting deluge of data.
Database: The Journal of Biological Databases and Curation provides an open access platform for the presentation of novel ideas in database research and biocuration, and aims to help strengthen the bridge between database developers, curators, and users.