Biotechnology Bulletin ›› 2014, Vol. 0 ›› Issue (5): 69-75.

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Identification of ZmCI-1B Promoter and Its Seven Deletions in Transgenic Arabidopsis thaliana

Li Ye1,2 Liu Xiaoqing2 Li Suzhen3 Zhou Xiaojin2 Yang Wenzhu2 Chen Rumei2   

  1. (1. School of Life Science and Engineering,Southwest University of Science and Technology,Mianyang 621010;2. Department of Crop Genomics & Genetic Improvement,Biotechnology Research Institute,Chinese Academy of Agricultural Sciences,Beijing 100081;3. Department of Agronomy,Agricultural University of Hebei,Baoding 071001)
  • Received:2014-02-20 Online:2014-05-23 Published:2014-05-24

Abstract: The expression vectors of ZmCI-1B promoter and its seven 5' truncated fragments were transformed into Agrobacterium tumefaciens strain GV3101. After identified by PCR assay, with Arabidopsis thaliana as genetic transformation, the expression vectors were transformed into Arabidopsis thaliana by floral-dip method. The transformed Arabidopsis thaliana plants were identified by PCR assay, then the seedings, flowers and siliques from positive plants were conducted to GUS histochemical staining. The results showed that the characterization of ZmCI-1B promoter in Arabidopsis thaliana is different from miaze. The ZmCI-1B promoter and its seven 5' truncated promoter-GUS constructs had different GUS staining in transformed Arabidopsis thaliana plants, revealing that different-length promoter had different promoting activity. The cis-acting elements on the promoter may contribute to this.

Key words: Promoter 5&apos, truncated fragments, Arabidopsis thaliana, GUS, Staining