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    杨宁, 杨雄, 李国雷, 陈仲. 毛白杨碱性/中性转化酶基因PtoNIN1的克隆与功能研究[J]. 北京林业大学学报, 2023, 45(5): 35-46. DOI: 10.12171/j.1000-1522.20220171
    引用本文: 杨宁, 杨雄, 李国雷, 陈仲. 毛白杨碱性/中性转化酶基因PtoNIN1的克隆与功能研究[J]. 北京林业大学学报, 2023, 45(5): 35-46. DOI: 10.12171/j.1000-1522.20220171
    Yang Ning, Yang Xiong, Li Guolei, Chen Zhong. Cloning and functional study of the alkaline/neutral invertase gene PtoNIN1 in Populus tomentosa[J]. Journal of Beijing Forestry University, 2023, 45(5): 35-46. DOI: 10.12171/j.1000-1522.20220171
    Citation: Yang Ning, Yang Xiong, Li Guolei, Chen Zhong. Cloning and functional study of the alkaline/neutral invertase gene PtoNIN1 in Populus tomentosa[J]. Journal of Beijing Forestry University, 2023, 45(5): 35-46. DOI: 10.12171/j.1000-1522.20220171

    毛白杨碱性/中性转化酶基因PtoNIN1的克隆与功能研究

    Cloning and functional study of the alkaline/neutral invertase gene PtoNIN1 in Populus tomentosa

    • 摘要:
        目的  蔗糖转化酶作为植物蔗糖代谢过程中的关键酶,在植物生长发育过程中发挥着重要作用。本研究对毛白杨碱性/中性转化酶基因PtoNIN1进行同源基因克隆、生物信息学分析、基因表达分析和遗传转化研究,以期为进一步揭示毛白杨蔗糖代谢调控过程奠定基础。
        方法  基于毛果杨同源基因PtrNIN1对毛白杨碱性/中性转化酶成员PtoNIN1进行同源克隆和生物信息学分析,采用实时荧光定量PCR的方法对不同组织部位(根、茎、叶和成熟叶)和不同发育时期下雌雄花芽中PtoNIN1的基因表达量进行分析,同时构建过表达载体,并对模式植物拟南芥开展遗传转化研究。
        结果  PtoNIN1的编码区长度为2 073 bp,共编码690个氨基酸,蛋白分子量为77.80 kDa,含有糖苷酶超家族100(glycosyl-hydrolase-100 superfamily)的特征结构域,类属于线粒体型的转化酶成员,在根、茎、叶以及成熟叶和雌雄花芽中均具有明显表达,且随着雌雄花芽的发育呈现先下降后保持稳定的表达趋势。拟南芥遗传转化研究表明:PtoNIN1的过表达显著增加了转基因植株莲座叶、茎及角果的鲜质量,提高了茎及角果中蔗糖的含量,同时也提高了蔗糖代谢通路其他关键基因的表达。
        结论  毛白杨PtoNIN1属于线粒体型转化酶家族成员,在毛白杨各个组织部位均具有明显表达,且在雌雄花芽的发育前期具有特异地高表达,在拟南芥中过表达PtoNIN1可显著增加生物量。该研究为杨树转化酶成员功能验证提供了借鉴,为揭示杨树蔗糖代谢过程奠定了基础。

       

      Abstract:
        Objective  Sucrose invertase, as a key enzyme in plant sucrose metabolism, plays an important role in plant growth and development. In this study, PtoNIN1, an alkaline/neutral invertase, was selected to do detailed analysis, including gene cloning, bioinformatics, gene expression and genetic transformation analysis, and these results were helpful for clarifying the mechanism of sucrose metabolism in Populus tomentosa.
        Method  PtoNIN1 was obtained through the homologous cloning of PtrNIN1 in P. trichocarpa, and then bioinformatics analysis for PtoNIN1 was carried out. Gene expression of PtoNIN1 was conducted at different organs (leaf, stem, root and mature leaves) and different developmental stages of male and female flower buds. And overexpression vector of PtoNIN1 was constructed to carry out genetic transformation research on the model plant Arabidopsis thaliana.
        Result  The coding region of PtoNIN1 was 2 073 bp in length. The PtoNIN1 protein contained 690 amino acids, and its molecular mass was 77.80 kDa. PtoNIN1 contained a specific domain of glycosyl hydrolase supergene family 100. The phylogenetic analysis showed that it is the member of mitochondrial-type invertase cluster. PtoNIN1 was widely expressed in the plant, including roots, stems, leaves, mature leaves, male and female flower buds. Thereinto, the development stage of male and female flower buds had an influence on the expression of PtoNIN1. Genetic transformation studies in Arabidopsis showed that overexpression of PtoNIN1 significantly increased the fresh mass of rosette leaves, stems and siliques. The sucrose contents in stems and siliques of transgenic plants were also significantly increased. And higher expression patterns of other sucrose metabolism-related genes were found in transgenic plants when compared with wild-type plant.
        Conclusion  PtoNIN1 is the member of mitochondrial-type invertases in P. tomentosa. It is widely expressed in various tissues of poplar, and has a specific expression in the early developmental stage of male and female inflorescences. Overexpression of PtoNIN1 in Arabidopsis can significantly increase plant biomass accumulation. This study provides a reference for the functional verification of other invertases in poplar, and lays a foundation for revealing the sucrose metabolic process of poplar.

       

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