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人骨形态发生蛋白-2基因克隆及真核表达载体的构建
引用本文:周诺,黄旋平,廖妮,韦山良,梁飞新,麦华明.人骨形态发生蛋白-2基因克隆及真核表达载体的构建[J].华西口腔医学杂志,2007,25(5):487-489.
作者姓名:周诺  黄旋平  廖妮  韦山良  梁飞新  麦华明
作者单位:广西医科大学附属口腔医院口腔颌面外科, 广西南宁530021
基金项目:国家自然科学基金 , 广西自然科学基金
摘    要:目的克隆人骨形态发生蛋白- 2(hBMP2)基因片段,构建pcDNA3.1- hBMP2真核表达质粒。方法采用逆转录聚合酶链式反应(RT- PCR)技术,从人骨肉瘤中扩增出人骨形态发生蛋白- 2基因片段,通过DNA重组技术将该基因片段重组于pcDNA3.1真核表达载体上,构建pcDNA3.1- hBMP2重组质粒,通过用PCR扩增、酶切电泳分析及DNA测序的方法对重组DNA进行鉴定。结果经PCR扩增、酶切电泳分析和DNA测序证实,本实验构建的重组质粒目的基因片段为人BMP2- cDNA。结论本实验成功克隆了hBMP2基因并构建成其真核表达质粒。

关 键 词:骨形态发生蛋白-  2  基因克隆  真核表达载体  
文章编号:1000-1182(2007)05-0487-03
收稿时间:2007-10-25
修稿时间:2007-01-23

Cloning of human bone morphogenetic protein-2 gene and the construction of its eukaryotic expression vector
ZHOU Nuo,HUANG Xuan-ping,LIAO Ni,WEI Shan-liang,LIANG Fei-xin,MAI Hua-ming.Cloning of human bone morphogenetic protein-2 gene and the construction of its eukaryotic expression vector[J].West China Journal of Stomatology,2007,25(5):487-489.
Authors:ZHOU Nuo  HUANG Xuan-ping  LIAO Ni  WEI Shan-liang  LIANG Fei-xin  MAI Hua-ming
Affiliation:Dept. of Oral and Maxillofacial Surgery, Hospital of Stomatology, Guangxi Medical University, Nanning 530021, China
Abstract:Objective To clone human bone morphogenetic protein-2(hBMP2) gene and construct its eukaryotic expression vector pcDNA3.1-hBMP2. Methods Human BMP2 gene was amplified by RT-PCR method from human osteosarcoma cells and constructed into eukaryotic expression vector pcDNA3.1-hBMP2. The gene in the vector pcDNA3.1-hBMP2 was identified by PCR amplification, enzyme digestion and DNA sequencing. Results The cloned DNA was confirmed to be hBMP-2 gene. Conclusion In this study, hBMP2 gene is successfully cloned and its eukaryotic expression vector pcDNA3.1-hBMP2 is constructed, which provides the foundation of using BMP2 gene therapy to accelerate new bone formation in distraction osteogenesis.
Keywords:bone morphogenetic protein-2  gene clone  eukaryotic expression vector
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