Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (11): 222-229.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0173

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Cloning and Expression Characteristics Analysis of LkNiR Promoter from Larix kaempferi

WU Yu-jie, WANG Yu-qian, LIU Cui-shuang, YU Yu-xiao, GENG Jing-ze, GAI Ying()   

  1. 1.State Key Laboratory of Tree Genetics and Breeding, College of Biological Sciences and Biotechnology, Beijing Forestry University, Beijing 100083
    2.The Tree and Ornamental Plant Breeding and Biotechnology Laboratory of National Forestry and Grassland Administration, Beijing 100083
  • Received:2026-02-04 Online:2026-11-26 Published:2026-11-03
  • Contact: GAI Ying E-mail:gaiying@bjfu.edu.cn

Abstract:

Objective Nitrite reductase (NiR) is a key plant nitrogen assimilation enzyme that catalyzes nitrite reduction to ammonium nitrogen and ensures efficient nitrogen assimilation. This study investigated Larix kaempferiLkNiR promoter expression features and nitrite stress response mechanisms and provided theoretical support for breeding forest trees with high nitrogen use efficiency. Method The LkNiR promoter sequence was cloned from L. kaempferi genomic DNA, and screened for cis-acting elements using PlantCARE and PLACE databases. The LkNiR-GFP reporter vector was constructed, and transgenic tobacco as well as L. kaempferi hairy roots were obtained via Agrobacterium-mediated genetic transformation. Promoter activity was detected by PCR identification, fluorescence observation, and RT-qPCR assays. L. kaempferi seedlings were treated with 100 mmol/L sodium nitrite, and the LkNiR gene temporal expression pattern was analyzed via RT-qPCR. Result The full-length LkNiR gene promoter (Accession No.: PV700087) was 1 941 bp, containing core elements (e.g., TATA-box, CAAT-box), multiple hormone-responsive elements, and stress-responsive elements. Notably, the LkNiR promoter harbored nine cis-acting elements involved in nitrogen assimilation. The promoter exhibited tissue-preferential expression in transgenic tobacco, with 92.1% higher activity in roots than the CaMV35S promoter, and 103.3% higher activity in L. kaempferi hairy roots than the CaMV35S promoter. Under nitrite stress, LkNiR expression showed spatiotemporal divergence: roots displayed a rapid early response, stems exhibited a moderate response, and needles had the strongest and most sustained induction. Conclusion The LkNiR promoter exhibits significant root-preferential expression characteristics, its activity is induced by nitrite signaling and shows spatiotemporal differentiation features, and it plays a key regulatory role in nitrogen assimilation and stress response in L. kaempferi.

Key words: nitrite reductase, promoter, Larix kaempferi, hairy root, nitrogen assimilation, nitrite stress, cis-acting elements, expression analysis