Xiong K Y, Jin R Z, Hu K H, Ding D M
Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan.
Chin J Biotechnol. 1990;6(4):243-50.
Human growth hormone releasing factor (hGRF) gene has been synthesized and cloned. The sequence of the synthetic hGRF gene, consisting of preferred codons for expression in E. coli, was designed with the aid of computer programs. Six segments with lengths ranging from 39 to 51 nucleotides were synthesized by solid-phase phosphoramidite method. The entire gene of 141 base pairs was constructed by enzymatic ligation of all synthetic segments and then cloned into plasmid pUC-19. The positive colonies were confirmed by the screening of ampicillin resistance, inactive beta-galactosidase, and analyzing by use of restriction enzymes and dot-blot hybridization. The cloned gene was sequenced by M13 dideoxynucleotide chain termination method and proven correct.
人生长激素释放因子(hGRF)基因已被合成并克隆。合成的hGRF基因序列由在大肠杆菌中表达的优选密码子组成,借助计算机程序进行设计。通过固相亚磷酰胺法合成了六个长度在39至51个核苷酸之间的片段。通过对所有合成片段进行酶促连接构建了141个碱基对的完整基因,然后将其克隆到质粒pUC-19中。通过氨苄青霉素抗性筛选、无活性β-半乳糖苷酶以及使用限制性酶和斑点杂交分析来确认阳性菌落。通过M13双脱氧核苷酸链终止法对克隆基因进行测序并证明其正确。