Chen Yuhui, Zhao Lingxia, Shen Guoan, Cui Lijie, Ren Weiwei, Zhang Hui, Qian Hongmei, Tang Kexuan
Plant Biotechnology Research Center, Shanghai Key Laboratory of Agrobiotechnology, School of Agriculture and Biology, Fudan-Shanghai Jiao Tong University-Nottingham Plant Biotechnology R&D Center, Institute of Systems Biology, People's Republic of China.
Biotechnol Appl Biochem. 2008 Jan;49(Pt 1):51-6. doi: 10.1042/BA20070055.
Talpha1 (thymosin alpha 1) is important in treating immunodeficiency and other diseases. In order to study the feasibility of expressing Talpha1 in plants, as the first attempt, we designed and synthesized the Talpha1 gene according to the plant codon usage preference and constructed the 4xTalpha1 concatemer (four copies of a DNA sequence arranged end-to-end in tandem). The latter was inserted into Escherichia coli expression vector pQE30, resulting in a recombinant plasmid that was subsequently transformed into E. coli M15. The 4xTalpha1 concatemer protein was successfully expressed in E. coli in a soluble form. The expressed protein was purified and its bioactivity was analysed by MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide] assay. Preliminary results showed that the 4xTalpha1 concatemer protein could stimulate the mice spleen lymphocyte proliferation. This is the first report on the expression of 4xTalpha1 concatemer that was synthesized according to plant codon usage preference in an E. coli expression system. The present study provides the basis for expressing the synthesized active Talpha1 gene in plants in the future.
胸腺素α1(Talpha1)在治疗免疫缺陷及其他疾病方面具有重要作用。为研究在植物中表达Talpha1的可行性,作为首次尝试,我们根据植物密码子使用偏好设计并合成了Talpha1基因,并构建了4xTalpha1串联体(由四个DNA序列拷贝首尾相连串联排列而成)。将后者插入大肠杆菌表达载体pQE30中,得到重组质粒,随后将其转化至大肠杆菌M15中。4xTalpha1串联体蛋白在大肠杆菌中成功以可溶形式表达。对表达的蛋白进行纯化,并通过MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H-四唑溴盐] 法分析其生物活性。初步结果表明,4xTalpha1串联体蛋白能够刺激小鼠脾淋巴细胞增殖。这是关于按照植物密码子使用偏好合成的4xTalpha1串联体在大肠杆菌表达系统中表达的首次报道。本研究为未来在植物中表达合成的活性Talpha1基因奠定了基础。