Function of BrSOC1b gene in flowering regulation of Chinese cabbage and its protein interaction

被引:6
作者
Li, Xin [1 ,2 ]
Shen, Changwei [3 ]
Chen, Ruixiang [1 ,2 ]
Sun, Bo [1 ,2 ]
Li, Daohan [1 ,2 ]
Guo, Xinlei [1 ,2 ]
Wu, Chunhui [1 ,2 ]
Khan, Nadeem [4 ]
Chen, Bihua [1 ,2 ]
Yuan, Jingping [1 ,2 ]
机构
[1] Henan Inst Sci & Technol, Sch Hort & Landscape Architecture, Eastern HuaLan Ave, Xinxiang City 453003, Henan, Peoples R China
[2] Henan Engn Res Ctr Dev & Utilizat Characterist Hor, Xinxiang 453003, Peoples R China
[3] Henan Inst Sci & Technol, Sch Resources & Environm Sci, Xinxiang 453003, Peoples R China
[4] Global Inst Food Secur, Saskatoon, SK, Canada
基金
中国国家自然科学基金;
关键词
Chinese cabbage; Flowering time; Genetic transformation; Protein interaction; SOC1; MADS-BOX GENE; EXPRESSION; SOC1; OVEREXPRESSION; PATHWAYS; VERNALIZATION; TEMPERATURE; ORTHOLOG; CONSTANS;
D O I
10.1007/s00425-023-04173-5
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Main conclusionBrSOC1b may promote early flowering of Chinese cabbage by acting on BrAGL9 a, BrAGL9 b, BrAGL2 and BrAGL8 proteins.SOC1 is a flowering signal integrator that acts as a key regulator in controlling plant flowering time. This study focuses on the cloning of the open reading frame of SOC1b (BrSOC1b, Gene ID: Bra000393) gene, and analyzes its structure and phylogenetic relationships. Additionally, various techniques such as vector construction, transgenic technology, virus-induced gene silencing technology, and protein interaction technology were employed to investigate the function of the BrSOC1b gene and its interactions with other proteins. The results indicate that BrSOC1b consists of 642 bp and encodes 213 amino acids. It contains conserved domains such as the MADS domain, K (keratin-like) domain, and SOC1 box. The phylogenetic analysis reveals that BrSOC1b shares the closest homology with BjSOC1 from Brassica juncea. Tissue localization analysis demonstrates that BrSOC1b exhibits the highest expression in the stem during the seedling stage and the highest expression in flowers during the early stage of pod formation. Sub-cellular localization analysis reveals that BrSOC1b is localized in the nucleus and plasma membrane. Furthermore, through genetic transformation of the BrSOC1b gene, it was observed that Arabidopsis thaliana plants expressing BrSOC1b flowered earlier and bolted earlier than wild-type plants. Conversely, Chinese cabbage plants with silenced BrSOC1b exhibited delayed bolting and flowering compared to the control plants. These findings indicate that BrSOC1b promotes early flowering in Chinese cabbage. Yeast two-hybrid and quantitative real-time PCR (qRT-PCR) analyses suggest that BrSOC1b may participate in the regulation of flowering by interacting with BrAGL9a, BrAGL9b, BrAGL2, and BrAGL8 proteins. Overall, this research holds significant implications for the analysis of key genes involved in regulating bolting and flowering in Chinese cabbage, as well as for enhancing germplasm innovation in Chinese cabbage breeding.
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页数:15
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