Molecular Characterization and Activity Analysis of Promoters from Two Cucumber Translationally Controlled Tumor Protein Genes (CsTCTPs)
Yongbo Yu
College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang 110866, China.
Xiangnan Meng
College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang 110866, China.
Shumin Jia
College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang 110866, China.
Mengqi Qu
College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang 110866, China.
Zhangtong Ma
College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang 110866, China.
Haiyan Fan *
College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang 110866, China and Key Laboratory of Protected Horticulture of Ministry of Education, Shenyang Agricultural University, Shenyang 110866, China.
*Author to whom correspondence should be addressed.
Abstract
Aims: The aim of the paper was to isolate and characterize the promoters of two cucumber TCTP genes (CsTCTP1 and CsTCTP2) and evaluate their active domains.
Study Design: CsTCTP1 and CsTCTP2 promoter activity were analyzed under treatments with different exogenous hormones.
Place and Duration of Study: In 2017, these experiments were conducted in College of Bioscience and Biotechnology of Shenyang Agricultural University (Lab 240).
Methodology: CsTCTPpro::GUS constructs were generated by using double digests method. Transient expression was mediated by Agrobacterium tumefaciens GV3101. Histochemical and Fluorometric GUS Assays were follow by the biochemical method.
Results: Bioinformatics analysis revealed some hormone- and defense-related response elements. Histochemical and fluorometric GUS assays demonstrated that the 0.7-kb CsTCTP1 promoter (proT1-0.7kb) and 0.7-kb and 1.3-kb CsTCTP2 promoters (proT2-0.7kb and proT2-1.3kb) had strong transcriptional activity. In addition, we used exogenous hormones (abscisic acid [ABA], salicylic acid [SA], and ethylene [ETH]) for treatment. The results showed that proT1-0.7kb and proT2-1.3kb activity were upregulated in the ABA treatment group, suggesting that these promoter sequences may contain ABA-related response elements. However, in the SA and ETH treatment groups, the activity of all the promoter fragments of CsTCTP1 and CsTCTP2 declined to different degrees, suggesting that SA and ETH may have negative regulatory effects on CsTCTP1 and CsTCTP2 promoters.
Conclusion: Taken together, these results suggest that the proT1-0.7kb promoter of CsTCTP1 and proT2-1.3kb promoter of CsTCTP2 may contain ABA-related response elements, and SA and ETH may have negative regulatory effects on the CsTCTP1 and CsTCTP2 promoters. This study will help to further understand the expression patterns and the regulatory mechanism of gene transcriptional regulation.
Keywords: Bioinformatics, CsTCTP, fluorometric GUS assay, histochemical assay, promoter