中国农业科学 ›› 2025, Vol. 58 ›› Issue (19): 3985-3999.doi: 10.3864/j.issn.0578-1752.2025.19.014

• 园艺 • 上一篇    下一篇

狗枣猕猴桃AkNAC2的克隆及功能研究

邹霈怡(), 刘美艳, 王颖, 李然红()   

  1. 牡丹江师范学院生命科学与技术学院,黑龙江牡丹江 157011
  • 收稿日期:2025-04-18 接受日期:2025-07-14 出版日期:2025-10-01 发布日期:2025-10-10
  • 通信作者:
    李然红,E-mail:
  • 联系方式: 邹霈怡,E-mail:zoupeiyi@126.com。
  • 基金资助:
    黑龙江省自然科学基金(PL2024C023); 黑龙江省省属本科高校优秀青年教师基础研究支持计划(YQJH2023094); 牡丹江师范学院“十四五”双一流学科建设揭榜挂帅项目(MSYSYL2022015)

Cloning and Functional Study of AkNAC2 from Actinidia kolomikta

ZOU PeiYi(), LIU MeiYan, WANG Ying, LI RanHong()   

  1. College of Life Sciences and Technology, Mudanjiang Normal University, Mudanjiang 157011, Heilongjiang
  • Received:2025-04-18 Accepted:2025-07-14 Published:2025-10-01 Online:2025-10-10

摘要:

【目的】NAC转录因子是植物中最大的转录因子家族,在植物抵抗低温等非生物胁迫过程中发挥重要作用。狗枣猕猴桃是最耐寒的猕猴桃之一,基于狗枣猕猴桃转录组数据获得一个响应低温的NAC转录因子家族成员——AkNAC2,通过构建过表达和抑制表达株系进一步研究AkNAC2在低温响应中的功能,为培育猕猴桃抗寒品种提供可用的基因资源。【方法】以狗枣猕猴桃叶片cDNA为模板克隆AkNAC2,利用生物信息学方法分析其序列信息和蛋白结构特征;利用GFP标记技术对AkNAC2进行亚细胞定位;通过转录组数据获得AkNAC2的组织表达特异性信息,qRT-PCR技术检测AkNAC2对低温、盐与水淹胁迫的响应。构建AkNAC2烟草过表达株系和狗枣猕猴桃抑制表达株系,分别比较低温处理后各转基因株系与对照的表型、生理生化指标及CBF通路相关基因表达量变化。【结果】AkNAC2的CDS长为897 bp,具有NAC基因家族保守结构域。AkNAC2编码298个氨基酸组成的亲水性、酸性蛋白,其启动子序列含多个非生物胁迫响应元件。系统进化分析表明,AkNAC2与毛花猕猴桃NAC2蛋白亲缘关系较近。亚细胞定位显示,AkNAC2定位在细胞核内。AkNAC2在狗枣猕猴桃叶中表达量最高,其次为雌花、雄花、果实和茎,根中表达量最低;低温、盐与水淹胁迫均能诱导AkNAC2的表达,其中,AkNAC2对低温胁迫的响应最明显。通过农杆菌介导法获得6个烟草转基因株系,分别命名为OE1—OE6,其中,OE2、OE4与OE6的基因表达量较高,作为后续研究材料。在4 ℃处理下,与野生型相比,3个转基因烟草株系的相对电导率与丙二醛含量显著降低,可溶性糖与可溶性蛋白等保护性物质含量显著增加,过氧化物酶与超氧化物歧化酶活性显著增强,抗氧化能力提高,CBF通路相关基因(NbtICE1NbtCOR47NbtCBF1NbtCBF2NbtCBF3)表达量显著上调;通过瞬时转化法获得狗枣猕猴桃AkNAC2抑制表达株系,qRT-PCR表明,与野生型和空载组相比,抑制表达株系中AkNAC2的表达量显著降低,在处理第4天时,表达量达到最低,是野生型的0.40倍、空载组的0.34倍。4 ℃低温处理后,抑制表达株系的相对电导率与丙二醛含量显著升高,可溶性糖与可溶性蛋白等保护性物质含量显著降低,过氧化物酶与超氧化物歧化酶活性显著降低,CBF通路相关基因的(AkCBF1.1AkCBF3)表达量显著下调。【结论】克隆获得1个狗枣猕猴桃低温响应基因AkNAC2,它可能通过影响CBF通路关键基因的表达和降低氧化胁迫而正调控植物的抗寒性。

关键词: 狗枣猕猴桃, AkNAC2, 转录因子, 基因克隆, 农杆菌介导法, CBF通路

Abstract:

【Objective】The NAC transcription factors constitute the largest family of transcription factors in plants, and play an important role in plant resistance to abiotic stresses such as cold. Actinidia kolomikta is one of the most cold-resistant kiwifruits. Based on the transcriptome data of Actinidia kolomikta, a NAC transcription factor family member responding to cold-AkNAC2 was obtained. The function of AkNAC2 in cold response was further studied by constructing overexpression and inhibition expression lines, which provided available gene resources for cultivating cold-resistant kiwifruit varieties.【Method】The leaves cDNA of Actinidia kolomikta were used as experimental materials to clone AkNAC2, and its sequence information and protein structure were analyzed by bioinformatics. The subcellular localization of AkNAC2 was analyzed by GFP labeling. The tissue-specific expression information of AkNAC2 was obtained by transcriptome data, and the response of AkNAC2 to cold, salt and waterlogging stress was detected by qRT-PCR. The overexpression lines of AkNAC2 Nicotiana benthamiana and the inhibitory expression lines of Actinidia kolomikta were constructed. The phenotypic, physiological and biochemical indexes and the expression of CBF pathway related genes were compared between the transgenic lines and the control after cold treatment.【Result】The CDS length of AkNAC2 is 897 bp. and has a domain. AkNAC2 encoding 298 amino acids, was a hydrophilic acidic protein, its promoter contained multiple cis-elements related to abiotic stress. Phylogenetic analysis indicated that AkNAC2 was closely related to NAC2 of Actinidia eriantha. Subcellular localization showed that AkNAC2 is localized in the nucleus. The expression level of AkNAC2 was the highest in leaves, followed by pistillate flowers, staminate flowers, fruits and stems, and the lowest in roots. The expression of AkNAC2 could be induced by cold, salt and waterlogging stress, and the response of AkNAC2 to cold stress was the most obvious. Six Nicotiana benthamiana transgenic lines were obtained by Agrobacterium-mediated, named OE1-OE6, Among them, the gene expression levels of OE2, OE4 and OE6 were higher, which were used as follow-up research materials. Under 4 ℃, compared with wild-type Nicotiana benthamiana, the relative conductivity and malondialdehyde content of the three transgenic Nicotiana benthamiana lines were lower, the content of protective soluble sugar and soluble protein significantly increased, the activity of peroxidase and superoxide dismutase increased, and the antioxidant capacity significantly increased. The expression levels of CBF pathway-related genes (NbtICE1, NbtCOR47, NbtCBF1, NbtCBF2, NbtCBF3) were significantly up-regulated. The AkNAC2 inhibitory expression lines of Actinidia kolomikta were obtained by transient transformation. qRT-PCR showed that the expression of AkNAC2 in the inhibitory expression lines was significantly lower than that in the wild type and the empty vector group. On the 4th day of treatment, the expression level reached the lowest, which was 0.40 times that of the wild type and 0.34 times that of the empty vector group. After 4 °C low temperature treatment, the relative conductivity and malondialdehyde content of the inhibited expression lines were significantly increased, the contents of protective substances such as soluble sugar and soluble protein were significantly decreased, the activities of peroxidase and superoxide dismutase were significantly decreased, and the expression levels of CBF pathway-related genes (AkCBF1.1 and AkCBF3) were significantly down-regulated.【Conclusion】A low temperature response gene AkNAC2 of Actinidia kolomikta was cloned, it may positively regulate the cold resistance of plants by affecting the expression of key genes in the CBF pathway and reducing oxidative stress.

Key words: Actinidia kolomikta, AkNAC2, transcription factor, gene cloning, Agrobacterium-mediated, CBF pathway