数字农科院2.0

A novel wheat S1-bZIP gene, TabZIP11-D, confers stress resistance in Arabidopsis

文献类型: 外文期刊

作者: Lina Zhang;Zhen Yu;Xingyan Liu;Yaoyao Wang;Jing Luo;Yinghong Wang;Ning Yang;Jie Du;Lan Ding;Chuan Xia;Lichao Zhang;Xiuying Kong

作者机构:

关键词: Dimer;Freezing;Salt;TabZIP11-D;TaCDPK1/5/9-1/30/TaCIPK31;Transcription factor

期刊名称: Plant Physiology and Biochemistry

ISSN: 0981-9428

年卷期: 2025 年 224 卷

页码:

收录情况: SCIE(2025版)

摘要: Most subgroup S1 basic leucine zipper (bZIP) transcription factors (TFs) play a crucial role in the abiotic stress responses. However, their functions and molecular mechanisms remain poorly characterized in wheat (Triticum aestivum L.). In this study, we identified a novel subgroup S1 bZIP gene, designated TabZIP11-D, which was transcriptionally responsive to abscisic acid (ABA), salt, and cold stresses. TabZIP11-D encodes a nuclear-localized protein that lacks transcriptional activation activity in yeast. The Ca2+ blocker LaCl3 significantly suppressed the salt-induced expression of TabZIP11-D. TabZIP11-D interacted with the Ca2+-dependent protein kinases (TaCDPK1, TaCDPK5, TaCDPK9-1, and TaCDPK30) and the CBL-interacting protein kinase TaCIPK31. Overexpression of TabZIP11-D enhanced salt and freezing tolerance by modulating soluble sugar and proline accumulation, reducing hydrogen peroxide (H2O2) and malondialdehyde (MDA) contents, and regulating the expression levels of stress-responsive genes. Furthermore, TabZIP11-D formed a homodimer with itself and heterodimers with group C bZIP proteins. Modified yeast one-hybrid assays revealed that TabZIP14 and TabZIP36 significantly enhanced TabZIP11-D binding to the G-box cis-element in the promoter region of TaCBF1 gene. These findings demonstrate that TabZIP11-D heterodimerizes with TabZIP14/36 to regulate cold signaling by promoting the TaCBF1 transcription. TabZIP11-D functions as a positive regulator in the salt stress response by interacting with TaCDPK1/5/9-1/30 and TaCIPK31.

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