Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (9): 128-136.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0339

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NtWUN Negatively Regulates Tobacco Trichome Development

LIU Na-wei, QIAN Meng-ying, ZHANG Hong-ying, WANG Zhao-jun, CUI Hong, YAN Xiao-xiao()   

  1. College of Tobacco Science, Henan Agricultural University, Zhengzhou 450046
  • Received:2026-03-26 Online:2026-09-26 Published:2026-09-16
  • Contact: YAN Xiao-xiao E-mail:xiaoxyan@henau.edu.cn

Abstract:

Objective This study aimed to elucidate the mode of action of the transcription factor NtWUN in mediating jasmonic acid (JA) signaling and to clarify the internal mechanism by which this transcription factor regulates trichome growth and development in tobacco. The findings would provide a theoretical and experimental basis for further dissecting the molecular mechanism underlying JA-mediated development of plant epidermal structures. Method In the common tobacco cultivar K326, multiple approaches including homologous cloning, bioinformatic analysis, subcellular localization assay, and quantitative real-time PCR (RT-qPCR) were adopted to characterize the sequence features and protein structure of the NtWUN gene, determine its subcellular localization properties, and clarify its tissue-specific expression patterns as well as transcriptional responses to methyl jasmonate (MeJA) treatments at varying concentrations. Furthermore, overexpression and knockout lines of NtWUN were generated to functionally validate the biological roles of this gene. Result NtWUN has two homologous sequences, NtWUN-1 and NtWUN-2. The coding region of NtWUN-1 is 630 bp in length, encoding 209 amino acids, while that of NtWUN-2 is 636 bp, encoding 211 amino acids. Phylogenetic analysis indicated that NtWUN-1 is highly homologous to Nicotiana sylvestris, and NtWUN-2 is highly homologous to N. tomentosiformis; both are closely related to homologous genes in Lycium barbarum. Expression pattern analysis showed that both NtWUN-1 and NtWUN-2 were most highly expressed in leaves, followed by trichomes, stems, and flowers, with the lowest expression in roots. Following treatment with different concentrations of MeJA, the relative expression levels of both genes initially increased and then decreased. Both genes were strongly induced by MeJA at 24 h, with expression levels upregulated by 10.2-fold and 11.8-fold, respectively. Subcellular localization results showed that NtWUN-1 and NtWUN-2 were both localized in the nucleus. Observation of trichome morphology and density revealed that the NtWUN overexpression line (OE8) showed 37.5% and 35.7% reductions in long-stalked and short-stalked glandular trichomes, respectively, while the knockout line (KO2) exhibited 50.0% and 57.1% increases in these two trichome types. The trichome types in the above transgenic lines were not affected. Conclusion The transcription factor NtWUN negatively regulates JA-mediated development of long-stalked and short-stalked glandular trichomes in tobacco.

Key words: tobacco, NtWUN, long-stalked trichome, short-stalked trichome, trichome density, gene editing, overexpression, jasmonic acid