拟南芥异源过表达木薯MeNRT2.6基因对氮素利用效率的影响

    Effects of heterologously overexpressing Manihot esculenta Crantz MeNRT2.6 gene in Arabidopsis thaliana on nitrogen utilization efficiency

    • 摘要:
      目的 高亲和硝酸盐转运蛋白家族2(Nitrate transporter 2,NRT2)基因在低氮条件下上调表达可促进植物对氮素的有效吸收,对提升植物耐低氮胁迫能力至关重要。本研究聚焦木薯Manihot esculenta Crantz的 MeNRT2.6基因功能研究通过在拟南芥Arabidopsis thaliana中异源过表达MeNRT2.6,解析MeNRT2.6在氮素利用效率方面的功能,为提高氮素利用效率的定向分子育种提供理论和技术支撑。
      方法 以转录组筛选出的低氮条件下在木薯根、茎、叶中均具有较高表达的MeNRT2.6基因作为研究对象,以木薯C3品种的cDNA为模板进行PCR扩增获得MeNRT2.6基因片段。通过生物信息学和组织表达分析,并结合原生质体瞬时表达系统确定MeNRT2.6的表达组织和亚细胞定位模式。利用浸花法创制在拟南芥中异源过表达MeNRT2.6的转基因株系,测定转基因株系在低、高浓度硝态氮条件下生理指标以及4个氮代谢关键酶−硝酸还原酶(Nitrate reductase,NR)、亚硝酸还原酶(Nitrite reductase,NiR)、谷氨酰胺合成酶(Glutamine synthetase,GS)和谷氨酸合成酶(Glutamate synthase,GOGAT)的活性。
      结果 MeNRT2.6与毛果杨PtNRT2.7的亲缘关系最近,氨基酸序列相似性达74.5%;其启动子序列存在逆境和激素类顺式响应元件。MeNRT2.6蛋白定位于细胞膜。在0.5 mmol/L硝态氮处理下,MeNRT2.6根据不同处理方式分别在木薯根、茎、叶中被诱导表达;在39.5 mmol/L硝态氮处理下,MeNRT2.6基因只在叶中被诱导表达,而与处理方式无关。0.5 mmol/L硝态氮胁迫下异源过表达MeNRT2.6基因的拟南芥转基因株系的根长、株高、鲜质量增加,氮代谢关键酶GOGAT、NR活性显著提升。
      结论 木薯MeNRT2.6基因启动子区域存在低氮响应元件,在拟南芥中异源表达MeNRT2.6基因能提高植株的氮素利用效率,对木薯氮高效种质的开发具有参考意义。

       

      Abstract:
      Objective The high-affinity nitrate transporter family 2 (NRT2), when upregulated under low nitrogen conditions, enhances plants’ efficient nitrogen uptake and plays a crucial role in improving plant tolerance to low nitrogen stress. This study focused on functional characterization of the MeNRT2.6 gene in cassava (Manihot esculenta Crantz), by examining the effects of heterologous overexpression of cassava MeNRT2.6 in Arabidopsis thaliana on nitrogen use efficiency, to provide both theoretical foundation and technical support for targeted molecular breeding aimed at improving nitrogen utilization efficiency.
      Method The MeNRT2.6 gene, which was identified through transcriptome screening as being highly expressed in cassava roots, stems and leaves under low nitrogen conditions, was selected as the research subject. The MeNRT2.6 gene fragment was obtained by PCR amplification using cDNA from cassava cultivar C3 as template. Bioinformatics analysis and tissue expression profiling were performed, and the tissue expression pattern and subcellular localization of MeNRT2.6 were determined combining a protoplast transient expression system. The transgenic A. thaliana lines heterologously overexpressing MeNRT2.6 were generated via the floral dip method. The SPAD values and the activities of four key nitrogen metabolism enzymes, including nitrate reductase (NR), nitrite reductase (NiR), glutamine synthetase (GS), and glutamate synthase (GOGAT), under low and high nitrate conditions were measured.
      Result Phylogenetic analysis showed that MeNRT2.6 was most closely related to PtNRT2.7 from Populus trichocarpa, with 74.5% amino acid sequence similarity. Its promoter sequence contains stress- and hormone-responsive cis-elements. MeNRT2.6 protein was localized to the cell membrane. Under 0.5 mmol/L nitrate nitrogen treatment, MeNRT2.6 expression was induced in cassava roots, stems and leaves depending on the treatment method. Under 39.5 mmol/L nitrate nitrogen treatment, MeNRT2.6 expression was specifically induced in leaves regardless of treatment method. Furthermore, A. thaliana plants heterologously overexpressing MeNRT2.6 showed increased root length, plant height and fresh weight under 0.5 mmol/L nitrate nitrogen treatment, along with enhanced activities of key nitrogen metabolism enzymes GOGAT and NR.
      Conclusion The MeNRT2.6 promoter contains low nitrogen-responsive elements. Heterologous overexpression of MeNRT2.6 in A. thaliana improved nitrogen use efficiency, providing valuable insights for developing nitrogen-efficient cassava germplasms.

       

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