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园艺学报 ›› 2025, Vol. 52 ›› Issue (7): 1828-1842.doi: 10.16420/j.issn.0513-353x.2024-0674

• 遗传育种·种质资源·分子生物学 • 上一篇    下一篇

杨树PagNAC47及其启动子克隆与功能分析

苏玉婷, 王慧林, 赵盼, 周心怡, 郑淑雅, 刘冉, 郭惠红*()   

  1. 林木遗传育种全国重点实验室,北京林业大学生物科学与技术学院,北京 100083
  • 收稿日期:2024-10-15 修回日期:2025-04-21 出版日期:2025-07-23 发布日期:2025-07-23
  • 通讯作者:
  • 基金资助:
    科技创新2030—重大项目(2023ZD04057); 国家自然科学基金面上项目(31870650)

Cloning and Functional Analysis of PagNAC47 Gene and Its Promoter from Poplar

SU Yuting, WANG Huilin, ZHAO Pan, ZHOU Xinyi, ZHENG Shuya, LIU Ran, GUO Huihong*()   

  1. State Key Laboratory of Tree Genetics and Breeding,College of Biological Science and Technology,Beijing Forestry University,Beijing 100083,China
  • Received:2024-10-15 Revised:2025-04-21 Published:2025-07-23 Online:2025-07-23

摘要:

以84K杨(Populus alba × Populus glandulosa)为试材,克隆得到PagNAC47基因及其启动子。PagNAC47编码区全长1 107 bp,编码368个氨基酸,具有NAC转录因子家族典型的NAM结构域,与毛果杨(P. trichocarpa)PtrNAC47蛋白的同源性最高,为92.2%;PagNAC47启动子序列长度为1 794 bp,含TATA-box和CAAT-box启动子基本元件及生长素(IAA)响应元件等。RT-qPCR分析表明,PagNAC47在老根、次生茎和成熟叶中的表达水平显著高于在幼根、初生茎和幼叶中的表达水平,且在成熟叶中表达水平最高。通过PagNAC47特异启动子驱动GUS报告基因的检测,揭示PagNAC47主要在器官的维管组织和成熟叶中表达。将35S启动子连接PagNAC47转入84K杨发现,与野生型相比,过表达株系的株高、茎粗、次生木质部宽度与层数、导管和纤维细胞面积及形成层层数均显著增加,根中次生木质部也有类似的现象,净光合速率和叶绿素含量显著增加,光合性能增强。PagNAC47的表达受IAA抑制,且抑制作用随IAA浓度的增加逐步增强。

关键词: 杨树, PagNAC47, 表达模式, 次生木质部, 光合作用, IAA

Abstract:

The PagNAC47 gene and its promoter were cloned from 84K poplar(Populus alba × Populus glandulosa). Coding region of the PagNAC47 was 1 107 bp in length,encoding 368 amino acids,with a typical NAM domain of the NAC transcription factor family. It had the highest homology with the PtrNAC47 protein from P. trichocarpa,which was 92.2%. The promoter of PagNAC47 was 1 794 bp in length,containing the basic promoter elements of TATA-box and CAAT-box and auxin(IAA)response elements. RT-qPCR analysis showed that the expression level of PagNAC47 was significantly higher in old roots,secondary stems and mature leaves than that in young roots,primary stems and young leaves,and the expression level was the highest in mature leaves. Furthermore,detection of PagNAC47-specific promoter-driven GUS reporter gene revealed that the PagNAC47 was mainly expressed in vascular tissues of organs and mature leaves. The 35S promoter-linked PagNAC47 was transformed into 84K poplar,and it was found that transgenic poplar overexpressing PagNAC47 significantly increased plant height,stem thickness,secondary xylem width and layer,vessel and fiber cell area,and cambium layer compared with the wild type,and similar phenomena were also observed in the secondary xylem of roots. Compared with wild-type poplar,the net photosynthetic rate and chlorophyll content of overexpressing PagNAC47 84K poplar were significantly increased,and the photosynthetic performance was enhanced. The expression of PagNAC47 was inhibited by IAA,and the inhibitory effect gradually enhanced with the increase of IAA concentration.

Key words: poplar, PagNAC47, expression pattern, secondary xylem, photosynthesis, IAA