小麦TabHLH123-6A基因克隆与功能标记开发
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作者单位:

1.山西农业大学农学院;2.中国农业科学院作物科学研究所;3.山西农业大学生命科学学院

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基金项目:

国家自然科学基金项目(31571611);黄土高原特色作物优质高效生产省部共建协同创新中心基金项目(SBGJXTZX-29)


Cloning and Functional Marker Development of Wheat Gene
Author:
Affiliation:

1.College of Agriculture, Shanxi Agricultural University;2.Institute of Crop Sciences, Chinese Academy of Agricultural Sciences;3.College of Life Scienas,Shanxi Agricultural University

Fund Project:

National Natural Science Foundation of China(31571611);Research Program Sponsored by Ministerial and Provincial CoInnovation Centre for Endemic Crops Production with High-quality and Efficiency in Loess Plateau(SBGJXTZX-29)

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    摘要:

    根系是植物吸收水分与养分的重要器官,挖掘利用小麦根系相关调控基因对于粮食生产具有重要意义。bHLH(basic Helix-Loop-Helix)是植物中广泛存在的一类转录因子,参与调节植物的生长发育。本研究克隆了小麦基因 TabHLH123-6A,其开放阅读框 1386 bp,编码 461 个氨基酸,含有保守的 HLH 结构域,具有典型的 bHLH 家族成员特性。对其互作蛋白预测分析发现,TabHLH123-6A 与 HLH 家族的其他蛋白以及锌指蛋白存在相互作用。组织表达模式分析表明,TabHLH123-6A 在小麦不同生育时期的各个组织中均有表达,在根和根基中表达量较高。启动子序列分析显示 TabHLH123-6A 启动子区含有多种顺式作用元件,包括生长素、脱落酸和茉莉酸甲酯等激素应答元件。qRT-PCR 检测结果表明在生长素、脱落酸和茉莉酸甲酯的处理下TabHLH123-6A 表达均上调,但是在 PEG 模拟的干旱处理下其表达受到抑制。利用小麦多态性群体材料检测到 TabHLH123-6A基因 25 bp 处有 1 个核苷酸变异位点(C/T),表示为 TabHLH12325-C/T,根据该位点开发了功能标记 dCAPS-KpnI。关联分析发现TabHLH12325-C/T 与小麦深根比显著相关,且等位变异类型为 TabHLH12325-C 的小麦深根比高于 TabHLH12325-T,TabHLH12325-T 在小麦育种历史中受到了正向选择。本研究结果为小麦根系构型改良提供了理论依据和基因资源。

    Abstract:

    The root system is a major organ for water and nutrient uptake. Exploration and utilization of the genes that regulate root development are important for enhancing wheat production. bHLH (basic Helix-Loop-Helix), a transcription factor family widely present in plants, plays an essential role in regulating the growth and development of plants. In this study, the TabHLH123-6A gene was isolated based on sequence homology, with an open reading frame of 1386 bp that encodes a protein comprises of 461 amino acids containing a conserved HLH domain. Based on the prediction of interacting proteins, TabHLH123-6A might be able to interact with HLH family members and zinc finger proteins. qRT-PCR analysis revealed the transcript of TabHLH123-6A in various tissues of wheat at different stages, with higher expression level in roots and root bases than that of other tissues. The promoter sequence analysis detected a number of cis-acting elements, including hormone response elements such as auxin, abscisic acid and methyl jasmonate. The expression of TabHLH123-6A was inducible under the treatments of auxin, abscisic acid or methyl jasmonate, but significantly repressed by PEG treatment. A nucleotide variation (C/T) at 25 bp of TabHLH123-6A gene (designated as TabHLH12325-C/T) was found using a panel of wheat accessions. A functional marker dCAPS-KpnI of TabHLH123-6A was developed to target this polymorphic site. Association analysis showed this polymorphism being significantly correlated with the ratio of deep root in wheat. The ratio of deep root with TabHLH12325-C allele is higher than that of TabHLH12325-T, and the frequency of TabHLH12325-T has been positively selected in the breeding process. Collectively, this study provided the theoretical basis and a locus for the improvement of wheat root system architecture.

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王晋萍,李 龙,贾小云,等.小麦TabHLH123-6A基因克隆与功能标记开发[J].植物遗传资源学报,2022,23(6):1782-1792.

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  • 收稿日期:2022-04-15
  • 最后修改日期:2022-04-26
  • 录用日期:2022-05-06
  • 在线发布日期: 2022-11-16
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