人GLUT4基因的克隆及原核表达的初步实验研究

目的　通过反转录聚合酶链方法 ,从人新鲜手术肌肉组织获得人葡萄糖转运子 4 (GLUT4 )cDNA基因 ,并分别克隆入测序载体、表达载体 ,获得具有正确序列的目的基因及其原核表达产物 ,为其进一步的抗体制备、活性鉴定及研究应用奠定物质基础。方法　经GenBank在线检索 ,设计、确定人GLUT4cDNA基因特异引物 ,采用反转录聚合酶链 (RT PCR)方法从一例手术的人新鲜腹部肌肉组织总RNA模板中 ,获得人GLUT4表达片段cDNA的基因 ,经克隆入测序载体pGEM 3zf(- )测序 ,验证cDNA大小、完整性及序列。再克隆入表达载体 pBV2 2 0 ,经温度诱导 ,在E .coli获得表达。结果　以设计的特异引物 ,从人肌肉组织模板中能得到预期大小完整的人GLUT4cDNA基因 ,并能插入预定的克隆载体中测序 ,所得基因的序列与目的基因的序列相符。所获GLUT4cDNA基因插入原核非融合表达载体pBV2 2 0 ,获得预期大小的重组表达产物。结论　从人肌肉组织中能获得具有正确序列、含完整起始及终止密码的人GLUT4cDNA基因。该人GLUT4cDNA基因的体外重组体能在原核表达系统表达

Cloning and expression of GLUT4 cDNA in E.coli

Objective To acquire glucose transporter 4 (GLUT4) cDNA from tissues of human muscle by RT-PCR, and to clone and express GLUT4 cDNA in E.coli. Methods GLUT4 cDNA primers were designed first and ascertained by detecting through Genbank on NCBI and DNA Star, then by using specific primers, the subjective cDNA segment was acquired by RT-PCR from human tissue. After that, it was cloned into cloning vector of pGEM-3zf(-) and sequenced automatically. Finally the subjective cDNA was cloned into vector of pBV220 and expressed in E.coli. Results The desired DNA could be acquired from tissues of human muscle by RT-PCR using special primers, the acquired cDNA fragment could be cloned into vector of pGEM-3zf(-) and sequenced. The GLUT4 cDNA sequence was highly conserved. GLUT4 cDNA could be expressed in E.coli, too. Conclusion The entire GLUT4 cDNA can be acquired from human muscular tissue by RT-PCR, and it can be expressed in E.coli.