Biotechnology Bulletin ›› 2025, Vol. 41 ›› Issue (6): 218-228.doi: 10.13560/j.cnki.biotech.bull.1985.2024-1182

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Cloning of MYB Transcription Factor Gene CeMYB154 and Analysis of Salt Tolerance Function in Cyperus esculentus

CHENG Shan1(), WANG Hui-wei1, CHEN Chen1, ZHU Ya-jing1, LI Chun-xin1, BIE Hai2, WANG Shu-feng1, CHEN Xian-gong1, ZHANG Xiang-ge1()   

  1. 1.Industrial Crop Research Institute, Henan Academy of Agricultural Sciences, Zhengzhou 450002
    2.Zhengzhou Institute of Agricultural Science and Technology, Zhengzhou 450002
  • Received:2024-12-05 Online:2025-06-26 Published:2025-06-30
  • Contact: ZHANG Xiang-ge E-mail:18790610677@163.com;maizezxg@163.com

Abstract:

Objective The MYB transcription factor gene CeMYB154 is involved in the salt stress response process in oil chestnut(Cyperus esculentus). Cloning and characterization of CeMYB154 gene in oil chestnut and analysis of its salt tolerance function may provide molecular basis and genetic resources for salt tolerant breeding of oil chestnut. Method Based on the reference genome information of oil chestnut, the full-length CDS sequence of CeMYB154 was cloned. Bioinformatics software was used to analyze its amino acid sequence characteristics and cis acting elements on its promoter, and molecular biology techniques were used to perform subcellular localization and transcriptional activation verification. CeMYB154 overexpression vector was constructed, Arabidopsis thaliana was transformed using Agrobacterium mediated method, and the salt-tolerant phenotype and physiological indicators of the overexpression strain were analyzed. Result The CeMYB154 CDS sequence with a length of 780 bp was successfully cloned, which encodes two typical MYB domains in the protein sequence and belongs to the R2R3 MYB transcription factor. Protein sequence alignment analysis showed that CeMYB154 protein is highly conserved across multiple species. The promoter region contains multiple hormone (such as ABA) response and MYB response related cis-acting elements. In addition, subcellular localization and transcriptional activation analysis showed that CeMYB154 is a nuclear transcription factor with transcriptional activation activity. Transgenic A. thaliana overexpressing CeMYB154 was successfully created and a homozygous T3 transgenic positive strain was obtained. Under salt stress, transgenic plant seedlings showed better growth status (leaf size, color, and root length) compared to wild-type A. thaliana. Moreover, the levels of MDA and H2O2 in the transgenic plants significantly reduced, while the activities of CAT, POD, and SOD antioxidant enzymes significantly enhanced, indicating that overexpression of the CeMYB154 gene improved salt tolerance in A. thaliana. Conclusion Preliminary evidence has shown that the CeMYB154 gene in C. esculentus has the function of positively regulating salt stress response. The overexpression of the CeMYB154 gene may enhance antioxidant enzyme activity and improve salt tolerance in transgenic plants.

Key words: Cyperus esculentus, salt stress, MYB transcription factor, transcriptional activation, functional analysis, over-expression, subcellular localization, antioxidase