中国农业科学

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最新录用:大豆红色种皮的色素鉴定和基因定位

曹杰1,2谷勇哲2洪慧龙2吴海涛2张霞2孙建强3包立高4邱丽娟1,2*
  

  1. 1吉林农业大学生命科学学院长春 130118;2中国农业科学院作物科学研究所北京 100081;3东北农业大学农学院,哈尔滨 1500304内蒙古自治区农牧业技术推广中心,呼和浩特 010018
  • 发布日期:2023-05-22

Pigment Identification and Gene Mapping in Red Seed Coat of Soybean

CAO Jie1,2, GU YongZhe2, HONG HuiLong2, WU HaiTao2, ZHANG Xia2, SUN JianQiang3, BAO LiGao4, QIU LiJuan1,2* #br#   

  1. 1 College of Life Sciences, Jilin Agricultural University, Changchun 130118; 2 Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081; 3 College of Agriculture, Northeast Agricultural University, Harbin 150030;4 Agriculture and Animal Husbandry Technology Promotion Center of Inner Mongolia Autonomous Region, Hohhot 010018
  • Online:2023-05-22

摘要: 【目的】揭示种子发育过程中种皮花青素(Anthocyanin)的含量变化以及导致泰兴矮脚红(TXAJH)红色种皮的主要花青素成分;定位控制花青素合成积累的关键基因,为深入了解红色种皮形成的调控机制奠定基础。【方法】利用超高效液相色谱串联质谱ultra-high performance liquid chromatography-tandem mass spectrometryUPLC-ESI-MS/MS)检测黄色种皮大豆绥农14SN14)和红色种皮大豆TXAJH不同发育阶段种皮的花青素成分与含量,分析与种皮颜色变化密切相关的花青素成分;利用SN14TXAJH杂交构建的重组自交系(recombinant inbred linesRIL)群体进行分离群体分组混合分析(bulked segregant analysisBSA,初步定位红色种皮相关基因的候选区域,在此基础上,结合标记连锁分析缩小候选区间并预测红色种皮候选基因;最后通过qRT-PCR验证候选基因的表达情况。【结果】检测SN14TXAJH 4个发育阶段的种皮,共发现12种花青素。在成分上,总花青素的聚类分析表明,TXAJHSN14之间以及TXAJH显色前后之间的种皮花青素组成均存在明显差异。在含量上,种子发育过程中,SN14种皮花青素的含量逐渐下降,而TXAJH种皮的含量迅速升高并保持稳定,种皮显色后,二者的花青素含量呈现极显著差异,在成熟阶段,TXAJH种皮花青素的含量是SN14200倍以上。矢车菊素-3-O-葡萄糖苷(Cyanidin-3-O-glucosideCy-3-glu)、芍药花素-3-O-葡萄糖苷(Peonidin-3-O-glucosidePn-3-glu)和牵牛花素-3-O-葡萄糖苷(Petunidin-3-O-glucosidePt-3-glu)是导致TXAJH种皮呈现红色的重要原因。BSA-seq关联分析将红色种皮基因的候选区间定位于第8染色体上,长度为8.66 Mb。利用27个多态性标记进行连锁分析得到10种单倍型,最终将候选区间缩小至702 kb。该区间中在亲本间存在非同义变异的基因共37个,其中,Glyma.08g059900编码MYB转录因子,Glyma.08g061300Glyma.08g063900编码bHLH转录因子,它们可能参与花青素的生物合成调控;Glyma.08g062000编码花青素还原酶1,可以将花青素转化为原花青素(proanthocyanidinPA)。基因表达分析结果表明,候选基因和花青素生物合成途径相关基因在SN14TXAJH中的表达模式相似,均为前者低于后者。种皮花青素主要成分与候选基因表达水平的关联分析结果显示二者之间存在极强的相关性。【结论】SN14TXAJH的种皮花青素组成存在差异,TXAJH红色种皮呈现红色可能是Cy-3-gluPn-3-gluPt-3-glu积累的结果预测Glyma.08g059900Glyma.08g061300Glyma.08g062000Glyma.08g063900为红色种皮候选基因,其中Glyma.08g059900Glyma.08g061300Glyma.08g063900可能对花青素生物合成途径的多个基因产生调控作用。


关键词: 种皮色, 花青素, BSA-seq, 基因定位, 转录因子

Abstract: 【Objective】To identify the key genes controlling anthocyanin synthesis and accumulation, to uncover changes in anthocyanin content of the seed coat during seed development, and the primary anthocyanin components responsible for the red seed coat of Taixingaijiaohong (TXAJH); and to lay the groundwork for a thorough understanding of the regulatory mechanism of red seed coat formation.【Method】Using ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-ESI-MS/MS), the anthocyanin composition and concentration of the yellow seed coat of soybean Suinong 14 (SN14) and the red seed coat of soybean TXAJH at various developmental stages were identified. The potential areas of red testa-related genes were first identified using bulked segregant analysis (BSA) on the recombinant inbred lines (RILs) made by crossing SN14 and TXAJH.  Based on this discovery, we performed marker linkage analysis to restrict the candidate intervals and predict the candidate genes, and qRT-PCR to confirm the expression of the anticipated candidate genes.【Result】When seed coats from the four developmental phases of SN14 and TXAJH were analyzed, a total of 12 anthocyanins were discovered. Cluster analysis of total anthocyanins revealed substantial changes in the seed coat's anthocyanin composition between TXAJH and SN14 as well as between TXAJH before and after color development. The anthocyanin content of the SN14 seed coat gradually decreased as the seed developed, whereas the TXAJH seed coat's content increased quickly and remained stable. After the development of the seed coat's color, the anthocyanin contents of SN14 and TXAJH showed highly significant differences, and at the mature stage, the TXAJH seed coat's anthocyanin content was more than 200 times that of SN14. The crimson coloring of the TXAJH seed coat was largely due to cyanidin-3-O-glucoside (Cy-3-glu), peonidin-3-O-glucoside (Pn-3-glu), and petunidin-3-O-glucoside (Pt-3-glu). The candidate interval for the red seed coat gene on chromosome 8 was discovered at 8.66 Mb by BSA-seq association analysis. 27 polymorphic markers were used in the marker linkage analysis, which produced 10 haplotypes and reduced the candidate interval to 702 kb. Nonsynonymous variations in 37 genes between the parents were found during this interval, These include the genes for encode the anthocyanin reductase 1 (Glyma.08g062000), the bHLH transcription factor (Glyma.08g061300 and Glyma.08g063900), and the MYB transcript factor (Glyma.08g059900). These genes may be involved in regulating the biosynthesis of anthocyanins, and anthocyanin reductase 1 can convert anthocyanins to proanthocyanidins (PA). The results of gene expression analysis revealed that candidate genes and genes related to the anthocyanin biosynthesis pathway had comparable expression patterns in SN14 and TXAJH, and both were expressed at lower levels in SN14 and at higher levels in TXAJH. It was discovered that there was a significant link between the principal constituents of seed coat anthocyanins and the level of candidate gene expression.【Conclusion】The anthocyanin makeup of SN14 and TXAJH's seed coats differed, and Cy-3-glu, Pn-3-glu, and Pt-3-glu may be to blame for the TXAJH's seed coat's red hue. According to predictions, Glyma.08g059900, Glyma.08g061300, Glyma.08g062000, and Glyma.08g063900 will likely be a candidate gene for the red seed coat, in which Glyma.08g059900, Glyma.08g061300, and Glyma.08g063900 may control a number of anthocyanin biosynthesis pathway genes.


Key words: seed coat color, anthocyanin, BSA-seq, gene mapping, transcription factors