大豆矮化突变体df1的候选基因鉴定

Candidate gene identification for soybean dwarf mutant df1

  • 摘要: 植物在外界物理与化学因素的胁迫下会产生基因突变。这种染色体基因组的变化不但能创造新的遗传变异材料,为植物遗传改良与育种服务,同时也是研究基因功能的重要技术手段。本研究对我国东北地区的大豆主栽品种黑河43进行伽玛射线诱变,获得极度矮化突变体 df1。遗传分析显示,df1突变为隐性单基因遗传。对杂合型衍生的df1突变型与正常野生型进行混池测序后,利用鉴定基因的 BVF-IGV流程,确定了位于1号染色体上包含69个基因的大片段缺失是引起 df1 突变的遗传因子。缺失区域序列开发的分子标记与表型间进行连锁分析及野生型与突变型混池的转录组分析结果,佐证了上述结论。根据本研究中野生型与突变型的基因表达谱以及公共资源中5000多份品种的转录组数据分析结果,最终确定 Glyma.01G066600 等26个基因为候选基因。研究结果为进一步通过精细定位克隆df1的功能基因以及明确其调控大豆生长发育的分子机理奠定了基础。

     

    Abstract: Genetic mutations can be induced by external physical and chemical factors. This chromosomal genomic change not only creates new genetic variation materials for genetic improvement and molecular breeding of plants, but also serves as an important technical tool for studying gene function. In this study, a dwarf mutant, df1, was identified in the mutant library generated by gamma radiation of the widely cultivated cultivar Heihe 43 in Northeast China. Genetic analysis indicated that the df1 mutation is controlled by a single recessive gene. By analyzing the resequencing data of df1 and wild-type bulked pools sampled from a segregating line using the BVF-IGV pipeline, a large fragment deletion containing 69 genes on chromosome 1 is identified as the causal genetic factor for the df1 mutation. Association analysis using molecular markers derived from the large fragment deletion and transcriptome analysis of RNA-seq data of bulked df1 and wild-type supports the above conclusion. Twenty-six candidate genes including Glyma.01G066600 are finally determined by combined analysis of gene expression profiles and over 5000 cultivars from the public database. The results of this study could facilitate the cloning of the functional gene for df1 mutation through fine-mapping and understanding of its molecular mechanism in regulating plant growth and development.

     

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